Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 071792
Company: WATSON LABS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
PROPRANOLOL HYDROCHLORIDE PROPRANOLOL HYDROCHLORIDE 90MG 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
07/15/1987 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
08/31/2001 SUPPL-13 Manufacturing (CMC)-Control

Label is not available on this site.

11/10/1999 SUPPL-12 Manufacturing (CMC)-Packaging

Label is not available on this site.

11/17/1999 SUPPL-11 Labeling

Label is not available on this site.

02/09/1999 SUPPL-10 Labeling

Label is not available on this site.

06/04/1992 SUPPL-9 Labeling

Label is not available on this site.

02/04/1991 SUPPL-8 Labeling

Label is not available on this site.

09/10/1990 SUPPL-4 Labeling

Label is not available on this site.

07/24/1990 SUPPL-3 Labeling

Label is not available on this site.

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