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GUJARAT FDA
US FDA issues Form 483 with 10 observations to Sun Pharma’s Halol unitListed pharmaceutical entity Sun Pharmaceutical Industries on Tuesday informed the exchanges that the US FDA has issued Form 483 with ten o...10 May, 2022, 11.47 AM IST- Bajaj Healthcare launches drug to treat black fungus infection in Covid patientsThe company has received approval from FDA (Food and Drugs Administration) Gandhi Nagar, Gujarat (India), to manufacture and market Posacon...28 May, 2021, 07.34 PM IST
- Covid-19: War of words over supply of oxygen in MaharashtraIn a letter addressed to Prime Minister Narendra Modi, Thackeray had said that medical oxygen requirement in the state is projected to reac...17 Apr, 2021, 09.49 PM IST
- Zydus Cadila gets EIR from USFDA for Ankleshwar facilityThe company's active pharmaceutical ingredient (API) manufacturing facility located at Ankleshwar (unit 1), Gujarat has received an Establi...23 Sep, 2019, 12.44 PM IST
- Sun Pharma receives 483 for Baska facility, co says responded to USFDAAt the conclusion of the inspection, the US FDA issued a Form 483, with one observation for which the Company has submitted the response to...25 Mar, 2019, 06.27 PM IST
- Alembic Pharma receives EIR from USFDAUSFDA releases a copy of the EIR to the establishment that was the subject of an FDA or FDA-contracted inspection when the agency determine...15 Jun, 2018, 11.13 AM IST
- Alkem Labs gets inspection report from USFDA for Gujarat API facilityThe US FDA has issued an establishment an inspection report for company's API manufacturing facility located at Ankaleshwar, said Alkem Lab...30 Mar, 2017, 12.47 AM IST
- Glenmark's Ankleshwar plant gets EIR report from USFDA"The EIR is issued by the FDA only if it finds the facility to be deemed acceptable," the company said in a BSE filing.15 Mar, 2017, 11.42 AM IST
- USFDA issues warning letter to Megafine Pharma for Vapi plantSummarising significant deviations from CGMP norms at the Vapi unit, the US Food and Drug Administration said that its investigators observ...08 Mar, 2017, 08.57 PM IST
- Alembic Pharma receives EIR report from USFDAUSFDA releases a copy of the Establishment Inspection Report to the establishment that was the subject of an FDA or FDA-contracted inspecti...05 Oct, 2016, 02.54 PM IST
- How faster USFDA nods will help Indian generic drug makersA long spell of sluggish approvals for generic drugs in the US may be nearing an end with early signs of a rebound.01 Sep, 2015, 04.43 AM IST
- After complaints, FDA collects samples from Amul godownFood and Drugs Administration (FDA) officials have raided Amul's godown here and took away six samples of its various milk products for tes...29 Jul, 2015, 08.09 PM IST
- USFDA issues warning to Indian drug maker Marck BiosciencesMarck Biosciences, now known as Amanta Healthcare received warning letter by US drug authority. USFDA found flase data and dead & decaying ...22 Aug, 2014, 12.21 PM IST
- Gujarat FDA recalls batch of diarrhea drug LoproGujarat FDA has stopped the sale of diarrhoea tablet Lopro, made by Danish Laboratories, after terming the drug sub-standard.31 May, 2012, 08.20 PM IST
- US to import cancer drug,Lipodox, from IndiaThe US said it will import cancer drug manufactured in India to overcome the acute shortage of the medicine used in treatment of ovarian, b...22 Feb, 2012, 01.20 PM IST
- Maharashtra FDA cracks whip on fake drug makersThe Maharashtra Food and Drug Administration (FDA) Intelligence wing has conducted raids on manufacturers of spurious thyroid drugs.20 Mar, 2007, 03.04 AM IST
- FDA raids fake thyroid drug makers in MumbaiThe State Food and Drug Administration (FDA) intelligence wing has conducted raids on manufacturers of spurious thyroid drugs and is lookin...20 Mar, 2007, 12.17 AM IST
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