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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 Oct 20, 2025

    50
    ›Oct 21, 2025approval313d agoDEFERASIROX — FDA approvalDEFERASIROX

    Sponsor: ACTAVIS ELIZABETH. Form: TABLET, FOR SUSPENSION. Route: ORAL

    full page →DEFERASIROX →fda approvals ↗
    ›Oct 21, 2025approval313d agoDEFERASIROX — FDA approvalDEFERASIROX

    Sponsor: ACTAVIS ELIZABETH. Form: TABLET, FOR SUSPENSION. Route: ORAL

    full page →DEFERASIROX →fda approvals ↗
    ›Oct 21, 2025approval313d agoDEFERASIROX — FDA approvalDEFERASIROX

    Sponsor: ACTAVIS ELIZABETH. Form: TABLET, FOR SUSPENSION. Route: ORAL

    full page →DEFERASIROX →fda approvals ↗
    ›Oct 21, 2025approval313d agoDEFERASIROX — FDA approvalDEFERASIROX

    Sponsor: ACTAVIS ELIZABETH. Form: TABLET, FOR SUSPENSION. Route: ORAL

    full page →DEFERASIROX →fda approvals ↗
    ›Oct 21, 2025approval313d agoDEFERASIROX — FDA approvalDEFERASIROX

    Sponsor: ACTAVIS ELIZABETH. Form: TABLET, FOR SUSPENSION. Route: ORAL

    full page →DEFERASIROX →fda approvals ↗
    ›Oct 22, 2025approval312d agoSIMPONI (GOLIMUMAB) — FDA approvalJanssen Biotech Inc

    Sponsor: CENTOCOR ORTHO BIOTECH INC. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Oct 22, 2025approval312d agoNICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE (NICARDIPINE HYDROCHLORIDE) — FDA approvalAmneal Pharmaceuticals, Inc.

    Sponsor: CAPLIN. Form: INJECTABLE. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Oct 22, 2025approval312d agoESMOLOL HYDROCHLORIDE — FDA approvalESMOLOL HYDROCHLORIDE

    Sponsor: SAGENT PHARMS INC. Form: INJECTABLE. Route: INJECTION

    full page →ESMOLOL HYDROCHLORIDE →fda approvals ↗
    ›Oct 22, 2025approval312d agoACETAMINOPHEN AND IBUPROFEN (ACETAMINOPHEN) — FDA approvalacetaminophen ER

    Sponsor: L PERRIGO CO. Form: TABLET. Route: ORAL

    full page →acetaminophen ER →fda approvals ↗
    ›Oct 22, 2025approval312d agoACETAMINOPHEN AND IBUPROFEN (ACETAMINOPHEN) — FDA approvalacetaminophen ER

    Sponsor: L PERRIGO CO. Form: TABLET. Route: ORAL

    full page →acetaminophen ER →fda approvals ↗
    ›Oct 22, 2025approval312d agoACETAMINOPHEN AND IBUPROFEN (ACETAMINOPHEN) — FDA approvalacetaminophen ER

    Sponsor: L PERRIGO CO. Form: TABLET. Route: ORAL

    full page →acetaminophen ER →fda approvals ↗
    ›Oct 22, 2025approval312d agoOXALIPLATIN — FDA approvalTeva Pharmaceuticals USA Inc

    Sponsor: NOVAST LABS. Form: INJECTABLE. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Oct 22, 2025approval312d agoCONTEPO (FOSFOMYCIN DISODIUM) — FDA approvalfosfomycin disodium

    Sponsor: MEITHEAL. Form: POWDER. Route: INTRAVENOUS

    full page →fosfomycin disodium →fda approvals ↗
    ›Oct 22, 2025approval312d agoVYEPTI (EPTINEZUMAB-JJMR) — FDA approvalH. Lundbeck AS

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

    full page →fda approvals ↗
    ›Oct 22, 2025approval312d agoVISINE (NAPHAZOLINE HYDROCHLORIDE) — FDA approval

    Sponsor: KENVUE BRANDS. Form: SOLUTION/DROPS. Route: OPHTHALMIC

    full page →fda approvals ↗
    ›Oct 22, 2025approval312d agoLOFEXIDINE HYDROCHLORIDE — FDA approvalLOFEXIDINE HYDROCHLORIDE

    Sponsor: NOVITIUM PHARMA. Form: TABLET. Route: ORAL

    full page →LOFEXIDINE HYDROCHLORIDE →fda approvals ↗
    ›Oct 22, 2025approval312d agoARIPIPRAZOLE — FDA approvalaripiprazole LA

    Sponsor: QUAGEN. Form: SOLUTION. Route: ORAL

    full page →aripiprazole LA →fda approvals ↗
    ›Oct 22, 2025recall312d agoAscend Laboratories, LLC recall (Cls II)Ascend Laboratories Ltd

    Atorvastatin Calcium Tablets USP, 80 mg, Rx Only, a). 90-count(NDC 67877-514-90), b). 500-count(NDC 67877-514-05), Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054 — Reason: Failed Dissolution Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoRising Pharma Holding, Inc. recall (Cls II)CHINA PHARMA HOLDINGS, INC.

    Carbidopa, Levodopa, Entacapone Tablets, 25 mg/100 mg/200 mg, 100-count bottle, Rx Only, Manufactured for: Rising Pharma Holdings, Inc. East Brunswick, NJ, 08816, Manufactured by Suven Pharmaceuticals Limited, Pashamylaram, Telangana, 205307, India. NDC# 16571-691-01 — Reason: Product mix up: complaint received that sealed medication bottle contained Carbidopa, Levodopa, and Entacapone film-coated tablets (37.5 mg/150 mg/200 mg) instead of labelled lower strength Carbidopa, Levodopa, and Entacapone film-coated tablets (25 mg/100 mg/200 mg). — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoVIONA PHARMACEUTICALS INC recall (Cls II)IONIS PHARMACEUTICALS INC

    Tavaborole Topical solution 5%, 10 mL bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Changodar, Ahmedabad, India, Distributed by: Viona Pharmaceuticals Inc., Cranford, NJ 07016, NDC 72578-102-04. — Reason: Discoloration — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoSTAQ Pharma, Inc. recall (Cls III)Silo Pharma, Inc.

    Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0156-02. — Reason: Labeling: Incorrect or Missing Lot and/or Exp Date — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoAscend Laboratories, LLC recall (Cls II)Ascend Laboratories Ltd

    Atorvastatin Calcium Tablets USP, 20 mg, Rx Only, a). 90-count(NDC 67877-512-90), b). 500-count (NDC 67877-512-05), c). 1000-count(NDC 67877-512-10),Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. — Reason: Failed Dissolution Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoAmerisource Health Services LLC recall (Cls II)AltrixBio Inc

    Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC 60687-695-01 - Carton NDC [60687-695-11- Unit Dose] — Reason: CGMP Deviations: The recalling firm filed for Chapter 11 on September 30, 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated. — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoASTRAZENECA PHARMACEUTICALS recall (Cls II)ASTRAZENECA PLC

    Fasenra (benralizumab) Injection, 30 mg/mL, one single-dose pre-filled syringe, Rx only, Manufactured by: AstraZeneca AB, Sweden, Distributed by: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850. NDC 0310-1730-30 — Reason: Lack of Assurance of Sterility: — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoIntegraDose Compounding Services LLC recall (Cls I)Revalesio Corp

    Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC, 719 Kasota Ave Se, Minneapolis, MN 55414-2842 NDC 71139-0012-1 — Reason: Subpotent Drug: Testing revealed there was no oxytocin in the IV bag. — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoAscend Laboratories, LLC recall (Cls II)Ascend Laboratories Ltd

    Atorvastatin Calcium Tablets USP, 10 mg, Rx Only a) 90-count bottle (NDC 67877-511-90), b). 500-count bottle (NDC 67877-511-05), c). 1000-count bottle (NDC 67877-511-10) Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. — Reason: Failed Dissolution Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoAscend Laboratories, LLC recall (Cls II)Ascend Laboratories Ltd

    Atorvastatin Calcium Tablets USP, 40 mg, Rx Only, a). 90-count (NDC 67877-513-90), b). 500-count (NDC 67877-513-05), c). 1000-count (NDC 67877-513-10), Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. — Reason: Failed Dissolution Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoSTAQ Pharma, Inc. recall (Cls III)Silo Pharma, Inc.

    Hydromorphone HCL PF, 10mg/50 mL (0.2mg/mL) in NACL, Injection for IV use, 50 mL Syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0104-05. — Reason: Labeling: Incorrect or Missing Lot and/or Exp Date — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoSTAQ Pharma, Inc. recall (Cls III)Silo Pharma, Inc.

    FentaNYL Citrate PF, 500mcg/50 mL (10mcg/mL) in NACL, Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0102-05. — Reason: Labeling: Incorrect or Missing Lot and/or Exp Date — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

    Viorele, Desogestrel and Ethinyl Estradiol, USP, 0.15 mg/ 0.02 mg and Ethinyl Estradiol Tablets, USP, 0.01 mg, 3 Blisters each containing 28 Tablets, Rx only, 28 day Regimen, Manufactured by: Glenmark Pharmaceuticals Limited, Colvale-Bardez, Goa 403513, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA., Mahwah, NJ, 07430, NDC 68462-318-29. — Reason: Failed Impurities/Degradation Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoEndo USA, Inc. recall (Cls III)Par Pharmaceutical Inc

    Everolimus tablets 5mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977, NDC 49884-125-91 — Reason: Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C. — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall312d agoSV Labs Prescott Corporation recall (Cls II)

    Aloe Up Sport Performance Sunscreen Lotion SPF 30, 1 FL OZ (30 mL) per tube, Mfd. for: ALOE UP, 9700 W. 76th St., Ste 112, Eden Prairie, Minnesota 55344 — Reason: cGMP deviations: the firm released and distributed product which failed total aerobic microbial count testing. — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 23, 2025approval311d agoVORICONAZOLE — FDA approvalVORICONAZOLE

    Sponsor: CADILA. Form: TABLET. Route: ORAL

    full page →VORICONAZOLE →fda approvals ↗
    ›Oct 23, 2025approval311d agoOMVOH (MIRIKIZUMAB-MRKZ) — FDA approvalmirikizumab

    Sponsor: ELI LILLY AND CO. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →mirikizumab →fda approvals ↗
    ›Oct 23, 2025approval311d agoJAVADIN (CLONIDINE HYDROCHLORIDE) — FDA approvalclonidine hydrochloride

    Sponsor: AZURITY. Form: SOLUTION. Route: ORAL

    full page →clonidine hydrochloride →fda approvals ↗
    ›Oct 23, 2025approval311d agoOLANZAPINE — FDA approvalolanzapine ODT

    Sponsor: DR REDDYS LABS LTD. Form: TABLET, ORALLY DISINTEGRATING. Route: ORAL

    full page →olanzapine ODT →fda approvals ↗
    ›Oct 23, 2025approval311d agoDALBAVANCIN HYDROCHLORIDE — FDA approvalFresenius Kabi USA LLC

    Sponsor: TEVA PHARMS INC. Form: POWDER. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Oct 23, 2025approval311d agoVORICONAZOLE — FDA approvalMylan Pharmaceuticals Inc

    Sponsor: MYLAN PHARMS INC. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 23, 2025approval311d agoBLENREP (BELANTAMAB MAFODOTIN-BLMF) — FDA approvalbelantamab mafodotin

    Sponsor: GLAXOSMITHKLINE LLC. Form: INJECTABLE. Route: INJECTION

    full page →belantamab mafodotin →fda approvals ↗
    ›Oct 23, 2025approval311d agoONDANSETRON HYDROCHLORIDE — FDA approvalondansetron hydrochloride CR

    Sponsor: RISING. Form: INJECTABLE. Route: INJECTION

    full page →ondansetron hydrochloride CR →fda approvals ↗
    ›Oct 23, 2025approval311d agoDEHYDRATED ALCOHOL — FDA approval

    Sponsor: ROYAL PHARMS. Form: SOLUTION. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Oct 23, 2025approval311d agoDESIPRAMINE HYDROCHLORIDE — FDA approvalDESIPRAMINE HYDROCHLORIDE

    Sponsor: INGENUS PHARMS LLC. Form: TABLET. Route: ORAL

    full page →DESIPRAMINE HYDROCHLORIDE →fda approvals ↗
    ›Oct 23, 2025approval311d agoDOCOSANOL — FDA approvalPL Developments Copiague LLC

    Sponsor: DR REDDYS. Form: CREAM. Route: TOPICAL

    full page →fda approvals ↗
    ›Oct 23, 2025approval311d agoQUINAPRIL HYDROCHLORIDE — FDA approvalLupin Ltd

    Sponsor: PHARMOBEDIENT. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 23, 2025approval311d agoQUINAPRIL HYDROCHLORIDE — FDA approvalLupin Ltd

    Sponsor: PHARMOBEDIENT. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 23, 2025approval311d agoOLANZAPINE — FDA approvalolanzapine ODT

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

    full page →olanzapine ODT →fda approvals ↗
    ›Oct 23, 2025approval311d agoONDANSETRON HYDROCHLORIDE — FDA approvalondansetron hydrochloride CR

    Sponsor: AUROBINDO PHARMA. Form: SOLUTION. Route: ORAL

    full page →ondansetron hydrochloride CR →fda approvals ↗
    ›Oct 23, 2025approval311d agoTOPIRAMATE — FDA approvalLP Pharmaceutical (Xiamen) Co Ltd

    Sponsor: ACTAVIS LABS FL. Form: CAPSULE, EXTENDED RELEASE. Route: ORAL

    full page →fda approvals ↗
    ›Oct 23, 2025approval311d agoTOPIRAMATE — FDA approvalLP Pharmaceutical (Xiamen) Co Ltd

    Sponsor: ACTAVIS LABS FL. Form: CAPSULE, EXTENDED RELEASE. Route: ORAL

    full page →fda approvals ↗
    ›Oct 24, 2025approval310d agoNEFFY (EPINEPHRINE) — FDA approvalInternational Medication Systems Ltd

    Sponsor: ARS PHARMS OPERATION. Form: SPRAY. Route: NASAL

    full page →fda approvals ↗
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    $IONS61.05-2.21%
    $SILO
    $SILO
    $AZN164.52-1.05%
    $SILO
    $RDY12.18+0.16%
    $LBRX47.73-0.33%
    $LLY1174.61-0.13%