U.S. flag An official website of the United States government
  1. Home
  2. Drug Databases
  3. Drugs@FDA

Drugs@FDA: FDA-Approved Drugs

Home | Previous Page

Abbreviated New Drug Application (ANDA): 074142
Company: TEVA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
NAPROXEN SODIUM NAPROXEN SODIUM EQ 250MG BASE TABLET;ORAL Discontinued None No No
NAPROXEN SODIUM NAPROXEN SODIUM EQ 500MG BASE 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
12/21/1993 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
10/15/1999 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

08/06/1998 SUPPL-6 Manufacturing (CMC)

Label is not available on this site.

06/23/1997 SUPPL-5 Manufacturing (CMC)

Label is not available on this site.

10/30/1996 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

10/30/1996 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

10/12/1995 SUPPL-2 Labeling

Label is not available on this site.

06/20/1994 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

Back to Top