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2025-12-06 01:45:01

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Latest News
  • Reliance Power Ltd clarifies on provisional attachment of assets by ED
  • Fino becomes India's first Payments Bank to receive 'In-principle' approval from RBI for conversion into a Small Finance Bank
  • Fire at Aditya Vision Ltd's warehouse
  • Shriram Pistons & Rings Ltd announces Definitive Agreement to acquire 100% stake in Antolin Group's Indian Operations
  • Supreme Petrochem Ltd announces temporary closure of plant at Manali, Chennai

Keywords Selected:  USFDA

Stock Report

  • Ipca Laboratories Ltd receives 3 observations from USFDA for API facility at Tarapur
  • Lupin receives tentative approval from U.S. FDA for Siponimod Tablets
  • Granules India's Packaging Facility in US Completes FDA inspection with Zero Observations
  • US FDA Accepts Wockhardt's New Drug Application for Breakthrough Antibiotic Zaynich
  • Glenmark Pharmaceuticals Ltd update on USFDA PAI at Chhatrapati Sambhajinagar Facility
  • Lupin Receives Approval from U.S. FDA for Biosimilar Armlupeg - Pegfilgrastim-unne
  • Zydus receives tentative approval from USFDA for Empagliflozin and Linagliptin Tablets, 10 mg/5 mg and 25 mg/5 mg
  • Glenmark Pharmaceuticals Receives Establishment Inspection Report (EIR) from U.S. FDA for its Monroe facility
  • SMS Pharmaceutical's associate company, VKT Pharma, receives US FDA approval for its reformulated Ranitidine
  • Zydus receives final approval from USFDA for Verapamil Hydrochloride Extended-Release Tablets USP, 120 mg, 180 mg and 240 mg
  • Shilpa Medicare Ltd receives 8 observations from USFDA for Unit 4 at Jadcherla
  • Lupin Ltd receives 7 observations from USFDA for Goa manufacturing facility
  • NATCO Pharma Ltd receives 7 Observations from USFDA for API unit at Manali, Chennai
  • Marksans Pharma Inc. receives USFDA approval for Loperamide Hydrochloride Tablets USP, 2 mg (OTC).
  • Solara announces successful closure of US FDA inspection of its Mangalore Facility with continued state of compliance on cGMP
  • Biocon Pharma Ltd receives approval from USFDA for its ANDA
  • Lupin announces closure of Inspection by U.S. FDA at its Nagpur Unit-1 Facility with No Observations
  • Alembic Pharmaceuticals Ltd announces USFDA Final Approval for Diltiazem Hydrochloride Tablets USP, 30 mg, 60 mg, 90 mg, and 120 mg
  • Zydus receives final approval from USFDA for Leuprolide Acetate injection, 14 mg/2.8 mL (1 mg/0.2 mL) multiple-dose vial
  • Aurobindo Pharma gets 9 observations from USFDA for Unit 2 of Eugia Pharma Specialities Ltd
  • USFDA inspects Unit 1 of Divi's Laboratories Limited
  • Closure of USFDA inspection at Zydus' oncology injectable manufacturing facility in SEZ1, Ahmedabad
  • Zydus receives final approval from USFDA for Diroximel Fumarate Delayed-Release Capsules, 231 mg
  • Alembic Pharmaceuticals Ltd announces USFDA Final Approval Dexlansoprazole Delayed Release Capsules, 30 mg and 60 mg

Latest Post

  • Reliance Power Ltd clarifies on provisional attachment of assets by ED
  • Fino becomes India's first Payments Bank to receive 'In-principle' approval from RBI for conversion into a Small Finance Bank
  • Fire at Aditya Vision Ltd's warehouse
  • Shriram Pistons & Rings Ltd announces Definitive Agreement to acquire 100% stake in Antolin Group's Indian Operations
  • Supreme Petrochem Ltd announces temporary closure of plant at Manali, Chennai


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