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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 070683
Company: SUN PHARM INDUSTRIES
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
OXAZEPAM OXAZEPAM 15MG TABLET;ORAL Discontinued None 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
01/16/1987 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
02/05/2021 SUPPL-14 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

04/28/2017 SUPPL-13 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

12/01/1998 SUPPL-12 Manufacturing (CMC)

Label is not available on this site.

12/23/1994 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

10/05/1993 SUPPL-10 Labeling

Label is not available on this site.

04/03/1992 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

04/03/1992 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

04/19/1989 SUPPL-6 Labeling

Label is not available on this site.

03/13/1990 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

09/04/1991 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

03/31/1987 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

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