Aurobindo Pharma has received the final approval from the US Food & Drug Administration (US FDA) to manufacture and market Norethindrone Acetate tablets USP, 5mg. The approved ANDA is bioequivalent ...

Glenmark Pharmaceuticals Ltd has informed BSE regarding a Press Release dated April 07, 2015, titled "Glenmark receives final ANDA approval for Norethindrone Acetate and Ethinyl Estradiol Tablets USP, ...

Aurobindo Pharma Limited today said it has received final approval from the US Food & Drug Administration to manufacture and market Norethindrone Acetate Tablets USP, in 5mg dosage. This is Aurobindo ...

"Glenmark Pharmaceuticals USA has been granted final approval by the US Food and Drug Administration (USFDA) for Norethindrone Acetate and Ethinyl Estradiol tablets USP and Ferrous Fumarate tablets, 1 ...

December 7, 2007 — The US Food and Drug Administration (FDA) has approved first-time generic formulations for nifedipine extended-release tablets in 90-mg strength for the management of angina and ...

Lupin has received final approval for its Fyavolv tablets (norethindrone acetate and ethinyl estradiol tablets usp, 0.5 mg/0.0025 mg and 1 mg/0.005 mg) from the United States Food and Drug ...

Aurobindo Pharma Ltd has received USFDA approval to manufacture and market Norethindrone Acetate tablets USP 5 mg, which is used in the treatment of endometriosis, uterine bleeding caused by abnormal ...

"Glenmark Pharmaceuticals USA has been granted final approval by USFDA for Hailey 24 Fe (Norethindrone Acetate and Ethinyl Estradiol tablets, USP and Ferrous Fumarate tablets), 1 mg/20 mcg, the ...

Aurobindo Pharma Ltd has informed BSE regarding a Press Release dated January 11, 2016 titled "Aurobindo Pharma receives USFDA Approval for Norethindrone Acetate Tablets".Source : BSE Advisory Alert: ...