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calendar

20,113 catalysts · 18,987 approval · 7,208 phase readout · 5,000 device 510k · 4,728 grant · 3,603 8k filing · 2,000 device pma

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  • approval18,987
  • phase readout7,208
  • device 510k5,000
  • grant4,728
  • 8k filing3,603
  • device pma2,000
  • device recall
2,000
  • recall1,126
  • device adverse event1,000
  • earnings585
  • therapy area

    no tagged catalysts yet

    Week of Mar 17, 2025

    12
    ›Mar 19, 2025recall529d agoCareFusion 213, LLC recall (Cls I)Coorg Instituite of Dental Sciences

    BD ChloraPrep Clear 1mL Applicators, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), Patient Preoperative Skin Preparation, Sterile Solution, 0.03 fl. oz (1 mL) each, 60 Applicators per Carton, CareFusion 213, LLC, El Paso, TX 79912, Subsidiary of Becton, Dickinson and Co., REF 930480, NDC 54365-400-31. — Reason: Non-Sterility: contamination of Aspergillus penicillioides, due to breach in package lidding. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 19, 2025recall529d agoAspen Biopharma Labs Pvt., Ltd. recall (Cls II)Greenstone LLC

    Voriconazole Container Description: voriconazole The product packed in white poly bag containing black poly bag and tied each individual finally packed in HDPE container for shipping. — Reason: CGMP Deviations — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 20, 2025approval528d agoBYLVAY (ODEVIXIBAT) — FDA approvalodevixibat

    Sponsor: IPSEN. Form: CAPSULE. Route: ORAL

    full page →odevixibat →fda approvals ↗
    ›Mar 20, 2025approval528d agoTREMFYA (GUSELKUMAB) — FDA approvalguselkumab

    Sponsor: JANSSEN BIOTECH. Form: INJECTABLE. Route: INJECTION

    full page →guselkumab →fda approvals ↗
    ›Mar 21, 2025approval527d agoNURTEC ODT (RIMEGEPANT SULFATE) — FDA approvalrimegepant sulfate ODT

    Sponsor: PFIZER. Form: TABLET, ORALLY DISINTEGRATING. Route: ORAL

    full page →rimegepant sulfate ODT →fda approvals ↗
    ›Mar 21, 2025approval527d agoPREZCOBIX (COBICISTAT) — FDA approvalGILEAD SCIENCES, INC.

    Sponsor: JANSSEN PRODS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Mar 21, 2025approval527d agoOTULFI (USTEKINUMAB-AAUZ) — FDA approvalOTULFI

    Sponsor: FRESENIUS KABI USA. Form: INJECTABLE. Route: INJECTION

    full page →OTULFI →fda approvals ↗
    ›Mar 21, 2025approval527d agoXTANDI (ENZALUTAMIDE) — FDA approvalenzalutamide

    Sponsor: ASTELLAS. Form: TABLET. Route: ORAL

    full page →enzalutamide →fda approvals ↗
    ›Mar 21, 2025approval527d agoXTANDI (ENZALUTAMIDE) — FDA approvalenzalutamide

    Sponsor: ASTELLAS. Form: CAPSULE. Route: ORAL

    full page →enzalutamide →fda approvals ↗
    ›Mar 21, 2025approval527d agoVYEPTI (EPTINEZUMAB-JJMR) — FDA approvalH. Lundbeck AS

    Sponsor: Lundbeck Seattle BioPharmaceuticals, Inc.. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Mar 21, 2025approval527d agoVYEPTI (EPTINEZUMAB-JJMR) — FDA approvalH. Lundbeck AS

    Sponsor: Lundbeck Seattle BioPharmaceuticals, Inc.. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Mar 21, 2025approval527d agoQULIPTA (ATOGEPANT) — FDA approvalatogepant

    Sponsor: ABBVIE. Form: TABLET. Route: ORAL

    full page →atogepant →fda approvals ↗

    Week of Mar 24, 2025

    38
    ›Mar 24, 2025approval524d agoSPRAVATO (ESKETAMINE HYDROCHLORIDE) — FDA approvalJanssen Therapeutics

    Sponsor: JANSSEN PHARMS. Form: SPRAY. Route: NASAL

    full page →fda approvals ↗
    ›Mar 24, 2025approval
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    page 328 of 403
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    524d ago
    ORLYNVAH (PROBENECID) — FDA approvalLannett Co Inc

    Sponsor: ITERUM THERAP. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Mar 25, 2025approval523d agoBLUJEPA (GEPOTIDACIN MESYLATE) — FDA approvalgepotidacin mesylate

    Sponsor: GLAXOSMITHKLINE. Form: TABLET. Route: ORAL

    full page →gepotidacin mesylate →fda approvals ↗
    ›Mar 25, 2025approval523d agoCONEXXENCE (DENOSUMAB-BNHT) — FDA approvalCONEXXENCE

    Sponsor: FRESENIUS KABI USA LLC. Form: INJECTION

    full page →CONEXXENCE →fda approvals ↗
    ›Mar 25, 2025approval523d agoTREMFYA (GUSELKUMAB) — FDA approvalguselkumab

    Sponsor: JANSSEN BIOTECH. Form: INJECTABLE. Route: INJECTION

    full page →guselkumab →fda approvals ↗
    ›Mar 26, 2025approval522d agoLORAZEPAM — FDA approvallorazepam ER

    Sponsor: RISING. Form: TABLET. Route: ORAL

    full page →lorazepam ER →fda approvals ↗
    ›Mar 26, 2025approval522d agoLORAZEPAM — FDA approvallorazepam ER

    Sponsor: RISING. Form: TABLET. Route: ORAL

    full page →lorazepam ER →fda approvals ↗
    ›Mar 26, 2025approval522d agoLORAZEPAM — FDA approvallorazepam ER

    Sponsor: RISING. Form: TABLET. Route: ORAL

    full page →lorazepam ER →fda approvals ↗
    ›Mar 26, 2025approval522d agoSTIMUFEND (PEGFILGRASTIM-FPGK) — FDA approvalSTIMUFEND

    Sponsor: FRESENIUS KABI USA. Form: SOLUTION. Route: INJECTION

    full page →STIMUFEND →fda approvals ↗
    ›Mar 26, 2025approval522d agoRINVOQ LQ (UPADACITINIB) — FDA approvalupadacitinib

    Sponsor: ABBVIE. Form: SOLUTION. Route: ORAL

    full page →upadacitinib →fda approvals ↗
    ›Mar 26, 2025approval522d agoRINVOQ (UPADACITINIB) — FDA approvalupadacitinib tartrate ER

    Sponsor: ABBVIE. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →upadacitinib tartrate ER →fda approvals ↗
    ›Mar 26, 2025approval522d agoCABOMETYX (CABOZANTINIB S-MALATE) — FDA approvalcabozantinib s-malate

    Sponsor: EXELIXIS INC. Form: TABLET. Route: ORAL

    full page →cabozantinib s-malate →fda approvals ↗
    ›Mar 26, 2025recall522d agoFruit Of The Earth, Inc. recall (Cls II)CVS HEALTH Corp

    CVS Health Concealing Acne Treatment Cream, CVS, 10% benzoyl peroxide, 1 oz (28 g), Distributed by: CVS Pharmacy, Inc — Reason: Chemical contamination: presence of benzene — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoAmgen, Inc. recall (Cls II)AMGEN INC

    Neupogen (filgrastim) For Injection, 300mcg/1 mL, 1 mL Single Dose Vials, Rx Only, For Subcutaneous or Intravenous Use Only, Sterile Solution - No Preservative, Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-530-01 (vial), NDC 55513-530-10 (box). — Reason: Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoMYLAN PHARMACEUTICALS INC recall (Cls II)MIRA PHARMACEUTICALS, INC.

    Prasugrel Tablets, USP, 5 mg, 30-count bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-5185-93 — Reason: Failed Dissolution Specifications - low dissolution results — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoFDC Limited recall (Cls II)FDC Ltd

    Ciprofloxacin Ophthalmic Solution USP, 0.3% as base, package in 5 mL bottles, Rx Only, Distributed by: Leading Pharma LLC, Fairfield, NJ. Manufactured by: FDC Limited, Maharashtra, India, NDC 69315-308-05 — 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 ↗
    ›Mar 26, 2025recall522d agoMylan Institutional, Inc. recall (Cls II)Mylan Institutional Inc

    Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per carton, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in India, NDC 51079-443-20. — Reason: Super-Potent Drug: Out of specification potency results were obtained. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoSlate Run Pharmaceuticals recall (Cls II)Slate Run Pharmaceuticals LLC

    Cinacalcet Hydrochloride Tablets 60 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-008-04 — Reason: CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoMEDLINE INDUSTRIES, LP - Northfield recall (Cls II)

    CURAD Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per Carton, 30 Boxes per Case, Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093, USA, Made in India, www.curad.com, 1-800-633-5463, NDC 53329-827-30. — Reason: Subpotent Drug — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoMEDLINE INDUSTRIES, LP - Northfield recall (Cls II)

    Medline Alcohol Prep Pads, 70% Isopropyl Alcohol, 100 Sterile 2-Ply Pads, Single Use Only, Large, www.medline.com, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093 USA, 1-800-MEDLINE, NDC 53329-811-30. — Reason: Subpotent Drug — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoFruit Of The Earth, Inc. recall (Cls II)Galderma Laboratories LP

    Walgreens Maximum Strength Tinted Acne Treatment Cream 10% Benzoyl Peroxide/Acne Medication, 0.65 oz (18.4g) tube in a carton; Distributed by: Walgreen CO., 200 Wilmot Rd., Deerfield, IL 60015 — Reason: Chemical contamination: presence of benzene — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoOne Source Nutrition, Inc, recall (Cls I)Shenzhen Hanhui Pharmaceutical Technology Co Ltd

    Vitality, Fast Acting Male Enhancement Product, Dietary Supplement, a) One Capsule per Packet, b) 6 capsules per bottle, Xtreme Potency. — Reason: Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared sildenafil and tadalafil. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoAmgen, Inc. recall (Cls II)AMGEN INC

    Neupogen (filgrastim) For Injection, 480 mcg/1.6 mL (300 mcg/1 mL), 1.6 mL single Dose Vial, Rx Only, For Subcutaneous or Intravenous Use Only, Sterile Solution - No Preservative, Amgen Inc. Thousand Oaks, CA 91320, NDC 55513-546-01 (vial), NDC 55513-546-10 (box). — Reason: Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoMylan Institutional, Inc. recall (Cls II)Mylan Institutional Inc

    Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per carton, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in India, NDC 51079-445-20. — Reason: Super-Potent Drug: Out of specification potency results were obtained. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoSlate Run Pharmaceuticals recall (Cls II)Slate Run Pharmaceuticals LLC

    Cinacalcet Hydrochloride Tablets 30 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-007-04 — Reason: CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoGolden State Medical Supply Inc. recall (Cls II)Apotex Corp

    PRASUGREL TABLETS, 5 mg, 30 tablet bottles, Rx only, packaged by GSMS, Incorporated, Camarillo, CA 93012 NDC 51407-444-30 — Reason: Failed Dissolution Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall522d agoRising Pharma Holding, Inc. recall (Cls II)CHINA PHARMA HOLDINGS, INC.

    Duloxetine Delayed-Release Capsules, USP, 30 mg, 1,000-count bottle, Rx only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC 57237-018-99 — Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 27, 2025approval521d agoDOXYCYCLINE HYCLATE — FDA approvalDOXYCYCLINE HYCLATE

    Sponsor: STRIDES PHARMA INTL. Form: TABLET. Route: ORAL

    full page →DOXYCYCLINE HYCLATE →fda approvals ↗
    ›Mar 27, 2025approval521d agoDOXYCYCLINE HYCLATE — FDA approvalDOXYCYCLINE HYCLATE

    Sponsor: STRIDES PHARMA INTL. Form: TABLET. Route: ORAL

    full page →DOXYCYCLINE HYCLATE →fda approvals ↗
    ›Mar 27, 2025approval521d agoDOXYCYCLINE HYCLATE — FDA approvalDOXYCYCLINE HYCLATE

    Sponsor: STRIDES PHARMA INTL. Form: TABLET. Route: ORAL

    full page →DOXYCYCLINE HYCLATE →fda approvals ↗
    ›Mar 27, 2025approval521d agoMETHADONE HYDROCHLORIDE — FDA approvalMETHADONE HYDROCHLORIDE

    Sponsor: VISTAPHARM LLC. Form: TABLET. Route: ORAL

    full page →METHADONE HYDROCHLORIDE →fda approvals ↗
    ›Mar 28, 2025approval520d agoPLUVICTO (LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN) — FDA approvallutetium Lu 177 vipivotide tetraxetan

    Sponsor: NOVARTIS. Form: SOLUTION. Route: INTRAVENOUS

    full page →lutetium Lu 177 vipivotide tetraxetan →fda approvals ↗
    ›Mar 28, 2025approval520d agoPLUVICTO (LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN) — FDA approvallutetium Lu 177 vipivotide tetraxetan

    Sponsor: NOVARTIS. Form: SOLUTION. Route: INTRAVENOUS

    full page →lutetium Lu 177 vipivotide tetraxetan →fda approvals ↗
    ›Mar 28, 2025approval520d agoABILIFY MAINTENA KIT (ARIPIPRAZOLE) — FDA approvalaripiprazole LA

    Sponsor: OTSUKA PHARM CO LTD. Form: FOR SUSPENSION, EXTENDED RELEASE. Route: INTRAMUSCULAR

    full page →aripiprazole LA →fda approvals ↗
    ›Mar 28, 2025approval520d agoACETAMINOPHEN AND CODEINE PHOSPHATE (ACETAMINOPHEN) — FDA approvalacetaminophen ER

    Sponsor: STRIDES PHARMA INTL. Form: TABLET. Route: ORAL

    full page →acetaminophen ER →fda approvals ↗
    ›Mar 28, 2025approval520d agoBRIXADI (BUPRENORPHINE) — FDA approvalbuprenorphine LA

    Sponsor: BRAEBURN. Form: SOLUTION, EXTENDED RELEASE. Route: SUBCUTANEOUS

    full page →buprenorphine LA →fda approvals ↗
    ›Mar 28, 2025approval520d agoACETAMINOPHEN AND CODEINE PHOSPHATE (ACETAMINOPHEN) — FDA approvalacetaminophen ER

    Sponsor: STRIDES PHARMA INTL. Form: TABLET. Route: ORAL

    full page →acetaminophen ER →fda approvals ↗
    ›Mar 28, 2025approval520d agoIMFINZI (DURVALUMAB) — FDA approvalASTRAZENECA PLC

    Sponsor: ASTRAZENECA UK LTD. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    $PFE27.96-0.21%
    $GILD145.68-2.14%
    $ABBV255.48-1.03%
    $ABBV255.48-1.03%
    $ABBV255.48-1.03%
    $EXEL55.26-1.50%
    $CVS
    $AMGN432.42-1.05%
    $MIRA0.9767-2.33%
    $AMGN432.42-1.05%
    $CPHI0.7101-0.82%
    $NVS153.81-0.54%
    $NVS153.81-0.54%
    $AZN164.52-1.05%