Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 070127
Company: DAVA PHARMS INC
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
07/30/1985 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
06/05/1991 SUPPL-12 Labeling

Label is not available on this site.

03/21/1991 SUPPL-11 Labeling

Label is not available on this site.

05/17/1989 SUPPL-10 Labeling

Label is not available on this site.

11/07/1988 SUPPL-9 Labeling

Label is not available on this site.

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