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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 071517
Company: SUPERPHARM
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
PROPRANOLOL HYDROCHLORIDE PROPRANOLOL HYDROCHLORIDE 40MG 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
06/08/1988 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
12/31/1990 SUPPL-5 Labeling

Label is not available on this site.

03/03/1989 SUPPL-4 Labeling

Label is not available on this site.

11/02/1988 SUPPL-3 Labeling

Label is not available on this site.

06/23/1988 SUPPL-1 Labeling

Label is not available on this site.

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