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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 091634
Company: GLENMARK PHARMS LTD
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ALYACEN 1/35 ETHINYL ESTRADIOL; NORETHINDRONE 0.035MG;1MG TABLET;ORAL-28 Prescription AB No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
01/19/2012 ORIG-1 Approval Not Applicable

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
07/06/2020 SUPPL-6 Labeling-Package Insert, Labeling-Patient Package Insert

Label is not available on this site.

07/06/2020 SUPPL-5 Labeling-Package Insert

Label is not available on this site.

05/16/2015 SUPPL-3 Labeling-Package Insert

Label is not available on this site.

03/29/2013 SUPPL-2 Labeling-Container/Carton Labels

Label is not available on this site.

07/31/2012 SUPPL-1 Labeling-Package Insert, Labeling-Container/Carton Labels

Label is not available on this site.

ALYACEN 1/35

TABLET;ORAL-28; 0.035MG;1MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
ALYACEN 1/35 ETHINYL ESTRADIOL; NORETHINDRONE 0.035MG;1MG TABLET;ORAL-28 Prescription No AB 091634 GLENMARK PHARMS LTD
DASETTA 1/35 ETHINYL ESTRADIOL; NORETHINDRONE 0.035MG;1MG TABLET;ORAL-28 Prescription No AB 090948 NOVAST LABS LTD
NORETHINDRONE AND ETHINYL ESTRADIOL ETHINYL ESTRADIOL; NORETHINDRONE 0.035MG;1MG TABLET;ORAL-28 Prescription No AB 206864 NAARI PTE LTD
NORETHINDRONE AND ETHINYL ESTRADIOL ETHINYL ESTRADIOL; NORETHINDRONE 0.035MG;1MG TABLET;ORAL-28 Prescription No AB 070687 WATSON LABS TEVA
NORTREL 1/35-28 ETHINYL ESTRADIOL; NORETHINDRONE 0.035MG;1MG TABLET;ORAL-28 Prescription No AB 072696 BARR
NYLIA 1/35 ETHINYL ESTRADIOL; NORETHINDRONE 0.035MG;1MG TABLET;ORAL-28 Prescription No AB 207056 AUROBINDO PHARMA
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