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14,069 catalysts · 3,313 8k filing · 2,402 grant · 2,299 approval · 1,631 device 510k · 1,179 device recall · 1,115 device pma

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  • 8k filing3,313
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  • approval2,299
  • device 510k1,631
  • device recall1,179
  • device pma1,115
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  • recall465
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    Week of Oct 6, 2025

    14
    ›Oct 10, 2025device recall309d agoMedline Industries, LP device recall (Cls I)

    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; OPEN HEART SUPPLEMENT DYNJ909116D; VASCULAR DYNJ909124F — Reason: Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 10, 2025device recall309d agoMedline Industries, LP device recall (Cls I)

    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; Product description/Product numbers: ADULT 120 EXPANDABLE W/MASK DYNJAA10591; ANES CIRC 120IN EXP-LF DYNJAA6555G; ANES CIRCUIT ADULT 120"-LF DYNJAA10817; ANESTHESIA 120" ADLT-LF DYNJAA10775; ANESTHESIA CIRC ADULT 120-LF DYNJAA10601; ANESTHESIA CIRCUIT - LF DYNJAA10261B; ANESTHESIA CIRCUIT 120EXP-LF DYNJAA10741A; ANESTHESIA CIRCUIT ADULT-LF DYNJAA0380A DYNJAA10641 DYNJAA10706B DYNJAA10851 DYNJAA10922B DYNJAA10971A DYNJAA11030A DYNJAA11087 DYNJAA11126; ANESTHESIA CIRCUIT-LF DYNJAA0309A DYNJAA0368A DYNJAA10368A DYNJAA10392 DYNJAA10430A DYNJAA10547A DYNJAA10639A DYNJAA10656A DYNJAA10685A DYNJAA10685B; CIRC 120" EXP 1 BV HMEF 3L GSL DYNJAA10920; EXPANDABLE CIRCUIT-LF DYNJAA11095; NM ANESTHESIA TURNOVER KIT DYNJAA0433; PROV HEALTH HEPA CIRC #2-LF DYNJAA0360; SPTMPX01IA CIRCUIT ADULT-LF DYNJAA10973A; — Reason: Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 10, 2025device recall309d agoMedline Industries, LP device recall (Cls I)

    DYNJ909119G ROBOTIC GASTRIC LAP SLEEVE-LF DYNJ909127F CYSTO DYNJ909129D GENERAL LAPAROSCOPY-LF — Reason: Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 10, 2025device recall309d agoMedline Industries, LP device recall (Cls I)

    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; ENT DYNJ909128I; LARYNGOSCOPY - BRONCHOSCOPY DYNJ909114D — Reason: Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 10, 2025device recall309d agoMedline Industries, LP device recall (Cls I)

    Convenience Kit, BREAST HERNIA DYNJ909125G — Reason: Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 10, 2025device recall309d agoMedline Industries, LP device recall (Cls I)

    Convenience kits; DYNJ901047R ORTHO SPINE FUMICH DYNJ902308K TOTAL JOINT DYNJ909111F DR SALMA'S SPINE DYNJ909117G PATTERSON TOTAL JOINT DYNJ909113F KYPHOPLASTY — Reason: Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 10, 2025device recall309d agoMedline Industries, LP device recall (Cls I)

    Convenience Kits: DYNJ901048N ORTHO SPINE ST CLAIR DYNJ909123F UROLOGY MINOR DYNJ909132F SET UP DYNJ909308D HIP PINNING — Reason: Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 10, 2025device recall309d agoMedline Industries, LP device recall (Cls I)

    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; BREATHING KIT-LF DYNJ10550 — Reason: Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 10, 2025device recall309d agoThoratec LLC device recall (Cls II)

    CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag Pre-connected Pack, REF: CMAEK00; CentriMag VAD KIT, REF: 201-51006, 201-51007, 201-90001 201-90001T; Blood Pump with CentriMag Acute Circulatory Support System for ECMO, REF: CMAEK01. CentriMag Blood Pump is a component to be used with CentriMag Acute Circulatory Support System — Reason: Acute circulatory support system pump may not fit into the motor and reports received of the pump not being securely locked into the motor using the screw-in locking feature. Failure to properly lock the pump into motor my not cause pump not inserted alarm, and could lead to particulate, increased heat, anxiety, inconvenience, delay in hemodynamic/ECMO support, stroke, embolism, death. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 10, 2025device recall309d agoMedline Industries, LP device recall (Cls I)

    Convenience kits; DYNJ901046M GYN ROBOTIC DYNJ909120D ROBOTIC PROSTATE — Reason: Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 10, 2025device recall309d agoMedline Industries, LP device recall (Cls I)

    Anesthesia circuit kit; CIRCUIT,ANES,EXTENDFLEX,120,LF DYNJAA10230 — Reason: Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 12, 2025device 510k307d agoInBios International, Inc. — COVID-19 Detect Rapid Self -Test (510k cleared)Synbio International, Inc.

    Product code: QYT. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 12, 2025device 510k307d agoShenzhen Nuon Medical Equipment Co., Ltd. — Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) (510k cleared)

    Product code: NFO. Advisory committee: Neurology. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 12, 2025device 510k307d agoPollogen, Ltd. — GENEO X ELITE (510k cleared)

    Product code: PAY. Advisory committee: General, Plastic Surgery. Type: Traditional

    full page →fda device 510k ↗

    Week of Oct 13, 2025

    36
    ›Oct 13, 2025device 510k306d agoBone Solutions, Inc. — Mg OSTEOINJECT™; Mg OSTEOREVIVE™; Mg OSTEOCRETE™ (510k cleared)UL Solutions Inc.

    Product code: MQV. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 13, 2025device recall
    ← prev
    page 4 of 282
    next →
    306d ago
    Paragon 28, Inc. device recall (Cls II)

    Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-S — Reason: Fibula nail system intended for use in fixation of fibular fractures and osteotomies, has out of specification thread depths on the fibula nail, so implant may not be able to mate properly with the associated mounting bolt. If nail (implant) cannot properly mate with instrumentation, the surgery potentially will need to be aborted. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 13, 2025device recall306d agoMRIMed Inc. device recall (Cls II)MARIMED INC.

    MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with SL-110, Mobile Exam Light — Reason: Due to battery component overheating while charging resulting in melting of internal components and causing smoke. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 13, 2025device recall306d agoDERMASENSOR INC device recall (Cls II)

    DermaSensor. Model/Catalog Number: 10101. Software Version: 3.0.2. Software-aided adjunctive diagnostic device for use by physicians on lesions suspicious for skin cancer — Reason: Potential for device to not meet specifications resulting in incorrect results or delay of referral for patients. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 13, 2025device recall306d agoTMJ Solutions Inc device recall (Cls I)TIC Solutions, Inc.

    TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only — Reason: Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 14, 2025approval305d agoWEGOVY (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 14, 2025approval305d agoSAXENDA (LIRAGLUTIDE) — FDA approvalNovo Nordisk Inc

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 14, 2025approval305d agoXULTOPHY 100/3.6 (INSULIN DEGLUDEC) — FDA approvalNovo Nordisk Inc

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 14, 2025approval305d agoEPINEPHRINE — FDA approvaladrenaline

    Sponsor: AMNEAL. Form: SOLUTION. Route: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    full page →adrenaline →fda approvals ↗
    ›Oct 14, 2025approval305d agoVICTOZA (LIRAGLUTIDE) — FDA approvalSaxenda

    Sponsor: NOVO NORDISK INC. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →Saxenda →fda approvals ↗
    ›Oct 14, 2025approval305d agoOZEMPIC (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 14, 2025approval305d agoOZEMPIC (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 14, 2025device 510k305d agoResponsive Arthroscopy, LLC — Mini Superhawk Suture Anchor System (510k cleared)

    Product code: MBI. Advisory committee: Orthopedic. Type: Special

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoDawell Medical, LLC — Lithoblast Single Use Holmium Laser Fibers (510k cleared)

    Product code: GEX. Advisory committee: General, Plastic Surgery. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoAsset Medikal — FlowArt® Vial Access Device Vented (510k cleared)

    Product code: LHI. Advisory committee: General Hospital. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoShenzhen Qiaochengli Technology Co., Ltd. — IPL Home Use Hair Removal Device (Models: FDA11, FDA12, FDA13, FDA14, FDA15, FDA16, FDA17, FDA18, FDA19, FDA20, FDA21S, FDA22S, FDA23S, FDA24S, FDA25, FDA26, FDA27, FDA28, FDA29S, FDA30S, FDA31S) (510k cleared)

    Product code: OHT. Advisory committee: General, Plastic Surgery. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoPureway Compliance, Inc. — PureWay Sharps Container 1-Gal, 2-Gal, 3-Gal (800011 800012, 800013) (510k cleared)

    Product code: MMK. Advisory committee: General Hospital. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoPhysio-Control, Inc. — LIFEPAK 15 AC Power Adapter (41577-000333) (510k cleared)

    Product code: MPD. Advisory committee: Cardiovascular. Type: Special

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoNexus Spine — PressON Spinal Fixation System (510k cleared)

    Product code: NKB. Advisory committee: Orthopedic. Type: Special

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoRapid Nexus Nanotech Wound Solutions, Inc. — Hemastyl(™) Wound Dressing (510k cleared)

    Product code: FRO. Advisory committee: Unknown. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoKeter Canada, Inc. — Community Containers (Flap and Daisy) (510k cleared)

    Product code: MMK. Advisory committee: General Hospital. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoMeta Systems Co., Ltd. — Demi Pro (510k cleared)

    Product code: EBZ. Advisory committee: Dental. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 14, 2025device pma305d agoShockwave Medical, Inc. — Shockwave™ lntravascular Lithotripsy {IVL) System with Shockwave C2/ C2+/ C2 Aero Coronary IVL Catheter (PMA supplement)

    Supplement type: 30-Day Notice. Product code: QMG. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Oct 14, 2025device pma305d agoPhysio-Control, Inc. — LIFEPAK 1000 defibrillator (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MKJ. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Oct 14, 2025device pma305d agoAdvanced Bionics — HiResolution™ Bionic Ear System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MCM. Advisory committee: EN. Decision: OK30

    full page →fda device pma ↗
    ›Oct 14, 2025device recall305d agoBecton Dickinson & Company device recall (Cls II)BECTON DICKINSON & CO

    BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341; — Reason: BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 14, 2025device recall305d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: EVIS EXERA III Duodenovideoscope Product Name: Olympus TJF-Q190V Model/Catalog Number: TJF-Q190V Product Description: This instrument is intended to be used with an Olympus video system center, light source, documentation equipment, monitor, EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery. — Reason: Continued reports of positive cultures and infections have identified updates to the reprocessing materials to minimize potential deviations in TJF duodenoscope reprocessing. Olympus is informing users of these changes, reminding users to closely follow the operation and reprocessing instructions, and providing updated materials to users. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 14, 2025device recall305d agoBeckman Coulter Ireland, Inc. device recall (Cls II)

    BECKMAN COULTER BICARBONATE REF: OSR6137 OSR6237 OSR6637 OSR6x37 Bicarbonate is a system reagent for the quantitative determination of Bicarbonate in human serum and plasma on Beckman Coulter AU analyzers. — Reason: Bicarbonate reagent may generate falsely high Bicarbonate results due to interference with Lactate Dehydrogenase (LDH) in the test sample. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 15, 2025approval304d agoCELECOXIB — FDA approvalCelebrex

    Sponsor: YILING. Form: CAPSULE. Route: ORAL

    full page →Celebrex →fda approvals ↗
    ›Oct 15, 2025approval304d agoCELECOXIB — FDA approvalCelebrex

    Sponsor: YILING. Form: CAPSULE. Route: ORAL

    full page →Celebrex →fda approvals ↗
    ›Oct 15, 2025approval304d agoFINTEPLA (FENFLURAMINE HYDROCHLORIDE) — FDA approvalfenfluramine hydrochloride

    Sponsor: UCB INC. Form: SOLUTION. Route: ORAL

    full page →fenfluramine hydrochloride →fda approvals ↗
    ›Oct 15, 2025approval304d agoLACOSAMIDE — FDA approvalLACOSAMIDE

    Sponsor: HETERO LABS LTD V. Form: TABLET. Route: ORAL

    full page →LACOSAMIDE →fda approvals ↗
    ›Oct 15, 2025approval304d agoLACOSAMIDE — FDA approvalLACOSAMIDE

    Sponsor: HETERO LABS LTD V. Form: TABLET. Route: ORAL

    full page →LACOSAMIDE →fda approvals ↗
    ›Oct 15, 2025approval304d agoLACOSAMIDE — FDA approvalLACOSAMIDE

    Sponsor: HETERO LABS LTD V. Form: TABLET. Route: ORAL

    full page →LACOSAMIDE →fda approvals ↗
    ›Oct 15, 2025approval304d agoLACOSAMIDE — FDA approvalLACOSAMIDE

    Sponsor: HETERO LABS LTD V. Form: TABLET. Route: ORAL

    full page →LACOSAMIDE →fda approvals ↗
    ›Oct 15, 2025approval304d agoLACOSAMIDE — FDA approvalLACOSAMIDE

    Sponsor: HETERO LABS LTD V. Form: TABLET. Route: ORAL

    full page →LACOSAMIDE →fda approvals ↗
    $SYIN
    $ULS
    $AMRX17.66+2.26%
    $NVO46.28-0.93%
    $MRMD
    $TIC9.7850-2.54%
    $BDX183.29+0.73%