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calendar

46 catalysts · 24 recall · 18 device 510k · 4 approval

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no tagged catalysts yet

Week of Dec 16, 2024

46
›Dec 18, 2024approval
621d ago
ENSACOVE (ENSARTINIB HYDROCHLORIDE) — FDA approvalensartinib hydrochloride

Sponsor: XCOVERY. Form: CAPSULE. Route: ORAL

full page →ensartinib hydrochloride →fda approvals ↗
›Dec 18, 2024approval621d agoIDACIO (ADALIMUMAB-AACF) — FDA approvalIDACIO

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

full page →IDACIO →fda approvals ↗
›Dec 18, 2024approval621d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

Sponsor: ELI LILLY AND CO. Form: CAPSULE. Route: ORAL

full page →selpercatinib →fda approvals ↗
›Dec 18, 2024approval621d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

Sponsor: ELI LILLY AND CO. Form: CAPSULE. Route: ORAL

full page →selpercatinib →fda approvals ↗
›Dec 18, 2024recall621d agoViatris Inc recall (Cls II)Viatris Inc

Levothyroxine Sodium Tablets USP, 150 mcg, packaged in a) 90-count bottles (NDC 0378-1815-77) and b) 1000-count bottles (NDC 0378-1815-10), 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, 2024recall621d agoViatris Inc recall (Cls II)Viatris Inc

Levothyroxine Sodium Tablets USP, 100 mcg, packaged in a) 90-count bottles (NDC 0378-1809-77) and b) 1000-count bottles (NDC 0378-1809-10), 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, 2024recall621d agoMylan Institutional, Inc. recall (Cls II)Mylan Institutional Inc

Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 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: 51079-443-20 — Reason: Subpotent and Superpotent Drug — Status: Ongoing

full page →fda recalls ↗
›Dec 18, 2024recall621d agoMylan Institutional, Inc. recall (Cls II)Mylan Institutional Inc

Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 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: 42292-040-20 — Reason: Subpotent and Superpotent Drug — Status: Ongoing

full page →fda recalls ↗
›Dec 18, 2024recall621d agoViatris Inc recall (Cls II)Viatris Inc

Levothyroxine Sodium Tablets USP, 50 mcg, packaged in a) 90-count bottles (NDC 0378-1803-77) and b) 1000-count bottles (NDC 0378-1803-10), 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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, 2024recall621d 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 510k621d agoCepheid® — Xpert MRSA/SA SSTI (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k621d 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 510k621d 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 510k621d 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 510k621d 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 510k621d agoSOADCO, S.L. — Klockner Kits (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k621d 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 510k621d agoViasonix , Ltd. — Falcon/Xpress (Falcon/Xpress) (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k621d 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 510k621d 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 510k621d agoDeltamed GmbH — 3Delta UNlimited (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k621d agoTeknimed Sas — GENTAFIX® (1, 3, 3MV) (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k621d 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 510k621d agoVentris Medical — Porous Biologic Scaffold (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k621d agoCaerus Corporation — Active System; Avenue8 (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k621d 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 510k621d 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 510k621d agoFreudenberg Medical, LLC — FirstFit Surgical Kit (510k cleared)

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

full page →fda device 510k ↗
$VTRS16.34-3.26%
$VTRS16.34-3.26%
$VTRS16.34-3.26%
$LLY1174.61-0.13%
$VTRS16.34-3.26%
$VTRS16.34-3.26%
$LLY1174.61-0.13%
$RDY12.18+0.16%
$VTRS16.34-3.26%
$ICFI90.22+0.47%
$VTRS16.34-3.26%
$VTRS16.34-3.26%
$VTRS16.34-3.26%
$VTRS16.34-3.26%
$POWL
$FOFO3.0000+2.39%
$VTRS16.34-3.26%