Search For "united states food amp drug administration"
Glenmark Pharma receives ANDA approval for Fluphenazine Hydrochloride Tabl
Updated : 2 years, 6 months ago IST
Mahwah (New Jersey) [US]/ Mumbai (Maharashtra) [India], November 7: Glenmark Pharmaceuticals Ltd. (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Fluphenazine Hydrochloride Tablets USP, 1 mg, 2.5 mg, 5 mg, and 10 mg, the generic versi
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Glenmark Pharmaceuticals receives sANDA approval for Tacrolimus Ointment,
Updated : 2 years, 9 months ago IST
Mumbai (Maharashtra) [India]/ Mahwah (New Jersey) [US], August 17: Glenmark Pharmaceuticals Ltd. (Glenmark), a research-led, integrated, global pharmaceutical company has received the final approval from the United States Food & Drug Administration (U.S. FDA) for Tacrolimus Ointment, 0.0
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Glenmark Pharmaceuticals receives sANDA approval for Abiraterone Acetate T
Updated : 4 years ago IST
Mumbai (Maharashtra) [India], May 20 (ANI/PRNewswire): Glenmark Pharmaceuticals Inc, USA (Glenmark) has received final approval by the United States Food & Drug Administration (US FDA) for Abiraterone Acetate Tablets USP, 500 mg, the generic version of Zytiga®1 Tablets, 500 mg, of J
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NeoImmuneTech obtains approval for phase 2 trial of brain tumor treatment
Updated : 4 years ago IST
Seoul [South Korea], May 12 (ANI/Global Economic): NeoImmuneTech said on the 11th that it has obtained the approval for a phase 2 clinical trial plan that concomitant administration of US Merck's immune checkpoint inhibitor Keytruda and its T-cell amplifier NT-I7 to patients with glioblastom
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Glenmark Pharmaceuticals receives tentative ANDA approval for Calcipotrien
Updated : 4 years ago IST
Mumbai (Maharashtra) [India], May 9 (ANI/PRNewswire): Glenmark Pharmaceuticals Inc., USA (Glenmark) has been granted tentative approval by the United States Food & Drug Administration (U.S. FDA) for Calcipotriene and Betamethasone Dipropionate Foam, 0.005 per cent|0.064 per cent, the gen
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Glenmark Pharmaceuticals receives ANDA approval for Lacosamide Tablets USP
Updated : 4 years, 2 months ago IST
Mumbai (Maharashtra) [India], March 21 (ANI/PR Newswire): Glenmark Pharmaceuticals Inc., USA (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for its Lacosamide Tablets1 USP, 50 mg, 100 mg, 150 mg and 200 mg, the generic version of Vimpat&
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Glenmark Pharmaceuticals receives ANDA tentative approval for Regadenoson
Updated : 4 years, 4 months ago IST
Mumbai (Maharashtra) [India], January 17 (ANI/PRNewswire): Glenmark Pharmaceuticals Inc., USA (Glenmark) has received tentative approval by the United States Food & Drug Administration (U.S. FDA) for Regadenoson Injection, 0.4 mg/5 mL (0.08 mg/mL) Single-Dose Pre-Filled Syringe, the g
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Glenmark Pharmaceuticals receives ANDA approval for Clindamycin Phosphate
Updated : 4 years, 8 months ago IST
Mumbai (Maharashtra) [India], September 21 (ANI/PR Newswire): Glenmark Pharmaceuticals Ltd. (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Clindamycin Phosphate Foam, 1%, the generic version of Evoclin®1 Foam, 1%, of Mylan Pharm
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Glenmark Pharmaceuticals receives ANDA tentative approval for Nintedanib C
Updated : 4 years, 11 months ago IST
Mumbai (Maharashtra) [India], June 25 (ANI/PRNewswire): Glenmark Pharmaceuticals Ltd (Glenmark) has received tentative approval by the United States Food & Drug Administration (U.S. FDA) for Nintedanib Capsules, 100 mg and 150 mg, the generic version of Ofev®1 Capsules, 100 mg and 1
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Glenmark Pharmaceuticals receives ANDA approval for Arformoterol Tartrate
Updated : 4 years, 11 months ago IST
Mumbai (Maharashtra) [India], June 23 (ANI/PRNewswire): Glenmark Pharmaceuticals Ltd (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Arformoterol Tartrate Inhalation Solution, 15 mcg/2 mL, Unit-Dose Vials, the generic version of BROVA
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Glenmark Pharmaceuticals receives ANDA approval for Theophylline Extended-
Updated : 4 years, 11 months ago IST
Mumbai (Maharashtra) [India], June 4 (ANI/PRNewswire): Glenmark Pharmaceuticals Ltd (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Theophylline Extended-release Tablets, 300 mg and 450 mg, bioequivalent and therapeutically equivalent
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Glenmark Pharmaceuticals receives ANDA approval for Icatibant Injection, 3
Updated : 5 years ago IST
Mumbai (Maharashtra) [India], May 24 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Icatibant Injection, 30 mg/3 mL (10 mg/mL) Single-Dose Prefilled Syringe, the generic version of F
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