Search For "united states food amp drug administration"
Glenmark Pharmaceuticals receives ANDA approval for Chlorpromazine Hydroch
Updated : 5 years, 2 months ago IST
Mumbai (Maharashtra) [India], March 24 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval from the United States Food & Drug Administration (US FDA) for Chlorpromazine Hydrochloride Tablets USP, 10 mg, 25 mg, 50 mg, 100 mg, and 200 mg, the generic v
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Glenmark Pharmaceuticals receives ANDA approval for Diltiazem Hydrochlorid
Updated : 5 years, 2 months ago IST
Mumbai (Maharashtra) [India], March 23 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Diltiazem Hydrochloride Extended-Release Capsules USP, 60 mg, 90 mg, and 120 mg, the generic ver
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Glenmark Pharmaceuticals receives ANDA approval for Topiramate Extended-re
Updated : 5 years, 3 months ago IST
Mumbai (Maharashtra) [India], February 3 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Topiramate Extended-Release Capsules, 25 mg, 50 mg, 100 mg, 150 mg, and 200 mg, the generic ve
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Glenmark Pharmaceuticals receives ANDA approval for Amphetamine Sulfate Ta
Updated : 5 years, 3 months ago IST
Mumbai (Maharashtra) [India], January 29 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Amphetamine Sulfate Tablets USP, 5 mg and 10 mg, the generic version of Evekeo®1 Tablets,
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Glenmark receives one ANDA approval and two tentative ANDA approvals - Tad
Updated : 5 years, 4 months ago IST
Mumbai (Maharashtra)[India], December 31 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark), a research-led global pharmaceutical company has received final approval by the United States Food & Drug Administration (U.S. FDA) for Tadalafil Tablets USP, 2.5 mg, 5 mg, 10 mg and 2
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Glenmark Pharmaceuticals receives ANDA tentative approval for Dabigatran E
Updated : 5 years, 5 months ago IST
Mumbai (Maharashtra) [India], December 21 (ANI/PRNewswire): Glenmark Pharmaceuticals Ltd (Glenmark) has received tentative approval by the United States Food & Drug Administration (U.S. FDA) for Dabigatran Etexilate Capsules, 75 mg, 110 mg, and 150 mg, the generic version of Pradaxa®
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Glenmark Pharmaceuticals receives ANDA approval for Tacrolimus Capsules US
Updated : 5 years, 6 months ago IST
Mumbai (Maharashtra) [India], November 11 (ANI/PRNewswire): Glenmark Pharmaceuticals Inc., USA (Glenmark) has been granted final approval by the United States Food & Drug Administration (U.S. FDA) for Tacrolimus Capsules USP, 0.5 mg, 1 mg and 5 mg, the generic version of Prograf®1 C
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Glenmark Pharmaceuticals receives ANDA approval for Sirolimus tablets, 0.5
Updated : 5 years, 7 months ago IST
Mumbai (Maharashtra) [India], Oct 19 (ANI/PRNewswire): Glenmark Pharmaceuticals Inc, USA (Glenmark) has received final approval by the United States Food & Drug Administration (US FDA) for Sirolimus Tablets, 0.5 mg, 1 mg and 2 mg, the generic version of Rapamune®1 Tablets, 0.5 mg, 1
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Glenmark Pharmaceuticals receives ANDA approval for Dimethyl Fumarate Dela
Updated : 5 years, 7 months ago IST
Mumbai (Maharashtra) [India] October 7 (ANI/PRNewswire): Glenmark Pharmaceuticals Inc, USA (Glenmark) has been granted final approval by the United States Food & Drug Administration (US FDA) for Dimethyl Fumarate Delayed-Release Capsules, 120 mg and 240 mg, the generic version of Tecfide
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