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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
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  • recall1,126
  • device adverse event1,000
  • earnings585
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    no tagged catalysts yet

    Week of Nov 24, 2025

    47
    ›Nov 25, 2025approval278d agoZEGERID OTC (OMEPRAZOLE) — FDA approvalCovis Pharmaceuticals Inc (Inactive)

    Sponsor: RILEY CONSUMER. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval278d agoENOXAPARIN SODIUM (PRESERVATIVE FREE) (ENOXAPARIN SODIUM) — FDA approvalenoxaparin sodium

    Sponsor: SHENZHEN TECHDOW. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →enoxaparin sodium →fda approvals ↗
    ›Nov 25, 2025approval278d agoIRBESARTAN — FDA approvalIRBESARTAN

    Sponsor: MACLEODS PHARMS LTD. Form: TABLET. Route: ORAL

    full page →IRBESARTAN →fda approvals ↗
    ›Nov 25, 2025approval278d agoSCEMBLIX (ASCIMINIB HYDROCHLORIDE) — FDA approvalasciminib hydrochloride

    Sponsor: NOVARTIS. Form: TABLET. Route: ORAL

    full page →asciminib hydrochloride →fda approvals ↗
    ›Nov 25, 2025approval278d agoVOYXACT (SIBEPRENLIMAB-SZSI) — FDA approvalsibeprenlimab

    Sponsor: OTSUKA PHARM CO LTD. Form: INJECTABLE. Route: INJECTION

    full page →sibeprenlimab →fda approvals ↗
    ›Nov 25, 2025approval278d agoIMFINZI (DURVALUMAB) — FDA approvalASTRAZENECA PLC

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

    full page →fda approvals ↗
    ›Nov 25, 2025approval278d agoACETAZOLAMIDE — FDA approvalAccord Healthcare Inc

    Sponsor: HIBROW HLTHCARE. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval278d agoCHILDREN'S CETIRIZINE HYDROCHLORIDE HIVES RELIEF (CETIRIZINE HYDROCHLORIDE) — FDA approvalKenvue Inc.

    Sponsor: BAJAJ. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval278d agoPERAMPANEL — FDA approvalCATALYST PHARMACEUTICALS, INC.

    Sponsor: TARO. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval278d agoNOREPINEPHRINE BITARTRATE — FDA approvalBaxter Healthcare Corp

    Sponsor: ANTHEA PHARMA. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Nov 25, 2025approval278d agoIRBESARTAN AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) — FDA approvalALDACTAZIDE

    Sponsor: MACLEODS PHARMS LTD. Form: TABLET. Route: ORAL

    full page →ALDACTAZIDE →fda approvals ↗
    ›Nov 25, 2025approval278d agoPERAMPANEL — FDA approvalPERAMPANEL

    Sponsor: MSN. Form: TABLET. Route: ORAL

    full page →PERAMPANEL →fda approvals ↗
    ›Nov 26, 2025approval277d agoVALBENAZINE TOSYLATE — FDA approvalVALBENAZINE TOSYLATE

    Sponsor: ZYDUS LIFESCIENCES. Form: CAPSULE. Route: ORAL

    full page →VALBENAZINE TOSYLATE →fda approvals ↗
    ›Nov 26, 2025approval277d agoDALBAVANCIN HYDROCHLORIDE — FDA approvalFresenius Kabi USA LLC

    Sponsor: KINDOS. Form: POWDER. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Nov 26, 2025approval277d agoCABENUVA KIT (CABOTEGRAVIR) — FDA approvalViiV Healthcare Company

    Sponsor: VIIV HLTHCARE. Form: SUSPENSION, EXTENDED RELEASE. Route: INTRAMUSCULAR

    full page →fda approvals ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    Lantiseptic, Skin Protectant, Lanolin USP 30%, packaged in a) 5g (0.17 oz) (NDC 61924-304-05), b)14.2g (0.5 oz)( NDC 61924-304-14), c) 4oz (NDC 61924-304-04), d) 4.5oz (NDC 61924-304-45), and e) 12oz (NDC 61924-304-12) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    KleenFoam Antimicrobial Foam Soap, Chloroxylenol 0.5%, 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-093-34 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)Insight Pharmaceuticals LLC

    DermaFungal, Antifungal Cream with 2% Miconazole Nitrate, packaged in a) 5 g (0.18 oz) per packet (NDC 61924-234-05), and b)106 g (3.75 oz.) per tube (NDC 61924-234-04) DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    DermaSarra, Camphor 0.5%, External Analgesic, 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    PeriGiene, Health Care Antiseptic, Chloroxylenol 0.5%, 222mL (7.5 fl. oz.) bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. 106 g (3.75 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-214-04 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC 61924-205-07) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    Renew PeriProtect, Zinc Oxide 12%, Dimethicone 1%, 113g (4 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-435-04 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoGolden State Medical Supply Inc. recall (Cls II)Avondale Pharmaceuticals LLC

    NIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle, Rx only, Manufactured by: Kremers Urban Pharmaceuticals, Inc., a subsidiary of Lannett Company, Inc., Seymour, IN 47274. Packaged by GSMS, Incorporated, Carmarillo, CA 93012. NDC: 51407-268-90 — Reason: Failed Dissolution Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E, Chloroxylenol 0.2%, packaged in a) 222 mL (7.5 fl. oz.) per tube (NDC 61924-092-08), b) 800 mL (27 fl. oz.) per bag (NDC 61924-092-27), and c 1000 mL (34 fl. oz.) per bag (NDC 61924-092-34), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-107-34 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoOtsuka ICU Medical LLC recall (Cls I)Upsher-Smith Laboratories LLC

    POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL Flexible Container, Highly concentrated 100 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26 — Reason: Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    UltraSure Anti-Perspirant & Deodorant, Aluminum Sesquichlorohydrate 15%, 118 mL (4 fl. oz.), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-266-04 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    GelRite Instant Hand Sanitizer, Alcohol 65%, packaged in a) 118 mL (NDC 61924-106-04), b) 473 mL (NDC 61924-106-16) and c) 800 mL (NDC 61924-106-27), and d) 1000 mL (NDC 61924-106-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    Hand-E-Foam, Benzethonium Chloride 0.20%, packaged in a) 236mL (NDC 61924-102-08) and b) 1000 mL (NDC 61924-102-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoOtsuka ICU Medical LLC recall (Cls I)Upsher-Smith Laboratories LLC

    POTASSIUM CHLORIDE Inj., 20 mEq total in 50 mL Flexible Container, Highly concentrated 400 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7077-14 — Reason: Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoPark Avenue Compounding recall (Cls II)Teva Pharmaceuticals USA Inc

    Fentanyl citrate, 2 mcg / ml / Ropivacaine, 0.2% in NS 150 mL, CII, 150 mL bag, Rx Only, Park Avenue Compounding, 3662 Park Ave, Saint Louis, MO, 63110, NDC 83863-4272-1. — Reason: CGMP Deviations: Revised interpretation of Acceptable Quality Level (AQL) results. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    Renew Skin Repair Cream, Dimethicone 1.5%, packaged in a) 5g tube (NDC 61924-405-05), b) 4 oz tube (NDC 61924-405-04), and c) 800 mL (NDC 61924-405-27), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    Lantiseptic, Dry Skin Therapy, Lanolin USP 30%, packaged in a) 5 g (0.17 oz) (NDC 61924-504-05), b) 4 oz (NDC 61924-504-04), and c)14 oz (NDC 61924-710-14) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoZydus Pharmaceuticals (USA) Inc recall (Cls II)LB PHARMACEUTICALS INC

    Bromocriptine Mesylate Capsules, USP, 5 mg, 30 Capsules per bottle, Rx Only. Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India. Distributed by: Zydus Pharmaceuticals, Pennington, NJ 08534. NDC 68382-110-06 — Reason: Failed Impurities/Degradation Specifications: Out of Specification (OOS) result reported for 2- Bromoergine impurity of Bromocriptine Mesylate Capsules. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    McKesson Skin Protectant, Lanolin USP, packaged in a) 5g (NDC 68599-6202-1), and b) 4oz NDC 68599-6203-4 tube, Distributed by McKesson Medical-Surgical Inc., Richmond, VA 23233. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoImprimis NJOF, LLC recall (Cls III)AbbVie Inc.

    Klarity-C Drops (Cyclosporine) 0.1%, Preservative-Free Sterile Ophthalmic Emulsion, This is a compounded drug, Office Use Only, 5.5 mL bottle, Rx only, Mfg by: Imprimis NJOF, LLC, 1705 Route 46 West, Ledgewood, NJ 07852, NDC 71384-514-05 — Reason: Subpotent Drug — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    4-N-1 Skin Protectant, No Rinse Wash Cream with Dimethicone 1%, 113g, (4 oz) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-208-04 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoAlembic Pharmaceuticals Limited recall (Cls III)Alembic Pharmaceuticals Inc

    Fesoterodine Fumarate, Extended-release Tablets, 4 mg, 30-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-175-30 — Reason: Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall277d agoDermaRite Industries, LLC recall (Cls II)

    DermaCerin, Skin Protectant Moisturizing Cream (petrolatum 33%), packaged in a) 106 g (3.75 oz.) per tube (NDC 61924-174-04) and b) 454 g (16 oz.) per jar (NDC 61924-174-16), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 28, 2025approval275d agoEPYSQLI (ECULIZUMAB-AAGH) — FDA approvalEPYSQLI

    Sponsor: SAMSUNG BIOEPIS CO LTD. Form: INJECTION. Route: SOLUTION

    full page →EPYSQLI →fda approvals ↗
    ›Nov 28, 2025approval275d agoIRBESARTAN AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) — FDA approvalALDACTAZIDE

    Sponsor: LUPIN LTD. Form: TABLET. Route: ORAL

    full page →ALDACTAZIDE →fda approvals ↗
    ›Nov 28, 2025approval275d agoIRBESARTAN AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) — FDA approvalALDACTAZIDE

    Sponsor: AUROBINDO PHARMA LTD. Form: TABLET. Route: ORAL

    full page →ALDACTAZIDE →fda approvals ↗
    ›Nov 28, 2025approval275d agoIRBESARTAN AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) — FDA approvalALDACTAZIDE

    Sponsor: HIKMA. Form: TABLET. Route: ORAL

    full page →ALDACTAZIDE →fda approvals ↗
    ›Nov 28, 2025approval275d agoCYCLOSPORINE — FDA approvalRestasis

    Sponsor: AMNEAL. Form: EMULSION. Route: OPHTHALMIC

    full page →Restasis →fda approvals ↗
    ›Nov 28, 2025approval275d agoIRBESARTAN AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) — FDA approvalPrinston Pharmaceutical Inc

    Sponsor: UNICHEM. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 28, 2025approval275d agoARMLUPEG (PEGFILGRASTIM-UNNE) — FDA approvalARMLUPEG

    Sponsor: LUPIN LTD. Form: INJECTION. Route: SOLUTION

    full page →ARMLUPEG →fda approvals ↗

    Week of Dec 1, 2025

    3
    ›Dec 1, 2025approval272d agoCEFAZOLIN SODIUM — FDA approvalSamson Medical Technologies LLC

    Sponsor: HIKMA FARMACEUTICA. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Dec 1, 2025approval
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    page 361 of 403
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    272d ago
    SELARSDI (USTEKINUMAB-AEKN) — FDA approvalAlvotech

    Sponsor: ALVOTECH USA INC. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Dec 1, 2025approval272d agoOMLYCLO (OMALIZUMAB-IGEC) — FDA approvalomalizumab biosimilar

    Sponsor: CELLTRION INC. Form: INJECTABLE. Route: INJECTION

    full page →omalizumab biosimilar →fda approvals ↗
    $NVS153.81-0.54%
    $AZN164.52-1.05%
    $KVUE19.20-0.10%
    $CPRX31.490.00%
    $LBRX47.73-0.33%
    $ABBV255.48-1.03%
    $AMRX17.54-2.61%
    $ALVO4.9500+1.43%