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calendar

22,353 catalysts · 4,728 grant · 4,406 device 510k · 3,288 8k filing · 3,188 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • device 510k4,406
  • 8k filing3,288
  • approval3,188
  • device pma2,000
  • device recall2,000
recall
1,078
  • device adverse event1,000
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
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    • Pulmonology22
    • Women's Health19
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    Week of Dec 16, 2024

    50
    ›Dec 18, 2024recall604d agoMylan Institutional, Inc. recall (Cls II)Mylan Institutional Inc

    Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-442-20 — Reason: Subpotent and Superpotent Drug — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoMylan Institutional, Inc. recall (Cls II)Mylan Institutional Inc

    Levothyroxine Sodium Tablets, USP, 150 mcg (0.150 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-445-20 — Reason: Subpotent and Superpotent Drug — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoMylan Institutional, Inc. recall (Cls II)Mylan Institutional Inc

    Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 42292-039-20 — Reason: Subpotent and Superpotent Drug — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoLNK International, Inc. recall (Cls II)ICF International, Inc.

    Kirkland Severe Cold & Flu Plus Congestion: Day - 112 coated caplets blister pack; (Acetaminophen 325mg, Dextromethorphan HBr 10 mg, Guaifenesin 200 mg, Phenylephrine HCl 5 mg); Night - 56 coated caplets blister pack; (Acetaminophen 325mg, Dextromethorphan HBr 10 mg, Doxylamine succinate 6.25 mg, Phenylephrine HCl 5 mg); Manufactured BY: LNK International, Inc. FOR: Costco Wholesale Corporation. NDC# 63981-795-81 — Reason: CGMP Deviations: Released product should have been rejected. — Status: Terminated

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoViatris Inc recall (Cls II)Viatris Inc

    Levothyroxine Sodium Tablets USP, 125 mcg, packaged in a) 90-count bottles (NDC 0378-1813-77) and b) 1000-count bottles (NDC 0378-1813-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoViatris Inc recall (Cls II)Viatris Inc

    Levothyroxine Sodium Tablets USP, 200 mcg, packaged in a) 90-count bottles (NDC 0378-1819-77) and b) 1000-count bottles (NDC 0378-1819-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoMylan Institutional, Inc. recall (Cls II)Mylan Institutional Inc

    Levothyroxine Sodium Tablets, USP, 137 mcg (0.137 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 42292-041-20 — Reason: Subpotent and Superpotent Drug — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoDr. Reddy's Laboratories, Inc. recall (Cls III)DR REDDYS LABORATORIES LTD

    Javygtor (sapropterin dihydrochloride) Tablets 100mg, 120-count bottle, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 Made in India, NDC 43598-096-04. — Reason: Failed Impurities/Degradation Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoAscend Laboratories, LLC recall (Cls II)Ascend Laboratories Ltd

    Dabigatran Etexilate, 150mg capsules, 60-count bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 NDC 67877-475-60 — Reason: CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended interim limit — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoAscend Laboratories, LLC recall (Cls II)Ascend Laboratories Ltd

    Dabigatran Etexilate, 75 mg capsules, 60-count bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 NDC 67877-474-60 — Reason: CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended interim limit — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoViatris Inc recall (Cls II)Viatris Inc

    Levothyroxine Sodium Tablets USP, 112 mcg, packaged in a) 90-count bottles (NDC 0378-1811-77) and b) 1000-count bottles (NDC 0378-1811-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoViatris Inc recall (Cls II)Viatris Inc

    Levothyroxine Sodium Tablets USP, 175 mcg, packaged in a) 90-count bottles (NDC 0378-1817-77) and b) 1000-count bottles (NDC 0378-1817-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoViatris Inc recall (Cls II)Viatris Inc

    Levothyroxine Sodium Tablets USP, 137 mcg, packaged in a) 90-count bottles (NDC 0378-1823-77) and b) 1000-count bottles (NDC 0378-1823-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoViatris Inc recall (Cls II)Viatris Inc

    Levothyroxine Sodium Tablets USP, 88 mcg, packaged in a) 90-count bottles (NDC 0378-1807-77) and b) 1000-count bottles (NDC 0378-1807-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoBiocompatibles UK, Ltd. recall (Cls III)BTG International Inc

    Varithena (polidocanol injectable foam) Administration Pack, Contains: 3 silicone-free syringes, 2 compression pads, 1 Varithena Transfer Unit, 1 manometer tubing, Rx Only, Distributed by Biocompatibles Inc., a BTG International Group company. CN01114.3 — Reason: Defective Delivery System: incorrect silicone oil-free NormJect 10 mL Luer Lock Solo syringes packaged in the pack, instead of the required silicone oil-free NormJect 10 mL Luer Solo syringes (luer slip connection). — Status: Terminated

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoMckesson Medical-Surgical Inc. Corporate Office recall (Cls II)Antares Pharma Inc

    Hylenex recombinant (hyaluronidase) injection, 150 USP units/mL, 4x1 mL Single Dose Vials, Rx only, Manufactured for and marketed by Halozyme, Inc., 12390 El Camino Real San Diego California 92130, Distributed by Antares Pharma, Inc., Ewing, NJ NDC 18657-117-04 — Reason: cGMP Deviations: Temperature excursion — Status: Terminated

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoFDC Limited recall (Cls II)FDC Ltd

    Timolol Maleate Ophthalmic Solution USP, 0.25%, Sterile, 15mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, NDC 64980-513-15. — Reason: Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle. — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoViatris Inc recall (Cls II)Viatris Inc

    Levothyroxine Sodium Tablets USP, 75 mcg, packaged in a) 90-count bottles (NDC 0378-1805-77) and b) 1000-count bottles (NDC 0378-1805-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024recall604d agoViatris Inc recall (Cls II)Viatris Inc

    Levothyroxine Sodium Tablets USP, 25 mcg, packaged in a) 90-count bottles (NDC 0378-1800-77) and b) 1000-count bottles (NDC 0378-1800-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 18, 2024device 510k604d agoCepheid® — Xpert MRSA/SA SSTI (510k cleared)

    Product code: NQX. Advisory committee: Microbiology. Type: Special

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoLima Corporate S.P.A. — Physica Porous Femoral Components (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoArtsmedia Denmark Aps — ARTSMedia Semen Wash Medium (510k cleared)

    Product code: MQL. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoArtsmedia Denmark Aps — ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100) (510k cleared)

    Product code: MQL. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoNatec Medical , Ltd. — Amethyst HP PTA OTW 0.035 Catheter (510k cleared)

    Product code: LIT. Advisory committee: Cardiovascular. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoSOADCO, S.L. — Klockner Kits (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoChongqing Moffy Innovation Technology Co., Ltd. — Respiratory Muscle Trainer (510k cleared)Hang Feng Technology Innovation Co., Ltd.

    Product code: BYI. Advisory committee: Anesthesiology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoViasonix , Ltd. — Falcon/Xpress (Falcon/Xpress) (510k cleared)

    Product code: JOP. Advisory committee: Cardiovascular. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoCadwell Industries, Inc. — Bluebird Single-Use Respiratory Effort Belt (510k cleared)POWELL INDUSTRIES INC

    Product code: MNR. Advisory committee: Anesthesiology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoChangsha Anxiang Medical Technology Co., Ltd. — Tens & Ems Device (TU1080) (510k cleared)

    Product code: NGX. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoDeltamed GmbH — 3Delta UNlimited (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoTeknimed Sas — GENTAFIX® (1, 3, 3MV) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoHunan Vathin Medical Instrument Co., Ltd. — Single-use Flexible Cystoscope (CY-E2E01, CY-E2E01R, CY-E2F01, CY-E2F01R, CY-E2G01, CY-E2G01R, CY-S2E01, CY-S2E01R); Digital Video Monitor (DVM-D1, DVM-D2) (510k cleared)

    Product code: FAJ. Advisory committee: Gastroenterology, Urology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoVentris Medical — Porous Biologic Scaffold (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoCaerus Corporation — Active System; Avenue8 (510k cleared)

    Product code: ILX. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoQuest Medical, Inc. — Lyka® PORT Needle Free Access Device (4170Y) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoEtex Corporation — EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone ) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 18, 2024device 510k604d agoFreudenberg Medical, LLC — FirstFit Surgical Kit (510k cleared)

    Product code: EWL. Advisory committee: Ear, Nose, Throat. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 19, 2024approval603d agoGABAPENTIN — FDA approvalGABAPENTIN

    Sponsor: STRIDES PHARMA. Form: CAPSULE. Route: ORAL

    full page →GABAPENTIN →fda approvals ↗
    ›Dec 19, 2024approval603d agoGABAPENTIN — FDA approvalGABAPENTIN

    Sponsor: STRIDES PHARMA. Form: CAPSULE. Route: ORAL

    full page →GABAPENTIN →fda approvals ↗
    ›Dec 19, 2024approval603d agoGABAPENTIN — FDA approvalGABAPENTIN

    Sponsor: STRIDES PHARMA. Form: CAPSULE. Route: ORAL

    full page →GABAPENTIN →fda approvals ↗
    ›Dec 19, 2024approval603d agoGABAPENTIN — FDA approvalAlmatica Pharma LLC

    Sponsor: ALKEM. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Dec 19, 2024approval603d agoCEREZYME (IMIGLUCERASE) — FDA approvalimiglucerase

    Sponsor: GENZYME. Form: INJECTABLE. Route: INJECTION

    full page →imiglucerase →fda approvals ↗
    ›Dec 19, 2024approval603d agoGABAPENTIN — FDA approvalGABAPENTIN

    Sponsor: SANDOZ. Form: CAPSULE. Route: ORAL

    full page →GABAPENTIN →fda approvals ↗
    ›Dec 19, 2024approval603d agoVEKLURY (REMDESIVIR) — FDA approvalremdesivir

    Sponsor: GILEAD SCIENCES INC. Form: SOLUTION. Route: INTRAVENOUS

    full page →remdesivir →fda approvals ↗
    ›Dec 19, 2024device 510k603d agoCardinalhealth — Monoject™ Enteral Syringe with ENFit Connector (401SE); Monoject™ Enteral Syringe with ENFit Connector (403SE); Monoject™ Enteral Syringe with ENFit Connector (406SE); Monoject™ Enteral Syringe with ENFit Connector (412SE); Monoject™ Enteral Syringe with ENFit Connector (435SE); Monoject™ Enteral Syringe with ENFit Connector (460SE) (510k cleared)CARDINAL HEALTH INC

    Product code: PNR. Advisory committee: Gastroenterology, Urology. Type: Special

    full page →fda device 510k ↗
    ›Dec 19, 2024device 510k603d agoWassenburg Medical, Inc. — System 83 Revolve Endoscope Washer/Disinfector (510k cleared)

    Product code: FEB. Advisory committee: Gastroenterology, Urology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 19, 2024device 510k603d agoVygon USA — Nutrifit (510k cleared)

    Product code: FPD. Advisory committee: Gastroenterology, Urology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 19, 2024device 510k603d agoYongkang Hengyi Vehicle Co., Ltd. — Electric Wheelchair (HC820N) (510k cleared)

    Product code: ITI. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 19, 2024device 510k603d agoStryker Neurovascular — Broadway 8 Catheter (510k cleared)

    Product code: QJP. Advisory committee: Cardiovascular. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 19, 2024device 510k603d agoJoytech Healthcare Co. , Ltd. — Electric Breast Pump (LD-208L, LD-3010L, LD-2010L, LD-3010, LD-2010) (510k cleared)NVP Healthcare Co Ltd

    Product code: HGX. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ← prev
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    $VTRS16.04-0.37%
    $VTRS16.04-0.37%
    $ICFI88.03-1.73%
    $VTRS16.04-0.37%
    $VTRS16.04-0.37%
    $VTRS16.04-0.37%
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    $VTRS16.04-0.37%
    $RDY12.42+0.24%
    $VTRS16.04-0.37%
    $FOFO3.0000+2.39%
    $POWL
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    $CAH231.24-1.25%