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2025-12-01 17:56:11

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Latest News
  • South West Pinnacle Exploration Ltd becomes accredited prospecting agency to explore it's own coal block in Jharkhand
  • Patel Retail Strengthens MMR Presence, Launches 48th Store in Mumbai Suburb
  • The Indian Link Chain Manufactures Ltd forms subsidiary RRP Technologies Ltd
  • Afcons receives EPC orders worth Rs 884 crore in November
  • East India Drums and Barrels Manufacturing Ltd receives LOA from Indian Oil Corporation Ltd

Keywords Selected:  USFDA

Stock Report

  • 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
  • Lupin Receives EIR from U.S. FDA for its Aurangabad (CSN) Facility
  • Lupin Bioresearch Center receives Zero Observations from U.S. FDA after Successful Inspection and Assessment
  • Zydus receives tentative approval from USFDA for Olaparib Tablets, 100 mg and 150 mg

Latest Post

  • South West Pinnacle Exploration Ltd becomes accredited prospecting agency to explore it's own coal block in Jharkhand
  • Patel Retail Strengthens MMR Presence, Launches 48th Store in Mumbai Suburb
  • The Indian Link Chain Manufactures Ltd forms subsidiary RRP Technologies Ltd
  • Afcons receives EPC orders worth Rs 884 crore in November
  • East India Drums and Barrels Manufacturing Ltd receives LOA from Indian Oil Corporation Ltd


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