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): 074495
Company: SANDOZ
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
12/05/1994 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
12/04/2000 SUPPL-9 Manufacturing (CMC)-Control

Label is not available on this site.

12/04/2000 SUPPL-8 Manufacturing (CMC)

Label is not available on this site.

03/27/2000 SUPPL-7 Manufacturing (CMC)-Control

Label is not available on this site.

03/27/2000 SUPPL-6 Manufacturing (CMC)-Control

Label is not available on this site.

03/27/2000 SUPPL-5 Manufacturing (CMC)-Facility

Label is not available on this site.

04/29/1996 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

06/24/1996 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

01/19/1996 SUPPL-2 Labeling

Label is not available on this site.

Back to Top