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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 017108
Company: SANDOZ
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
WESTADONE METHADONE HYDROCHLORIDE 2.5MG TABLET, DISPERSIBLE;ORAL Discontinued None No No
WESTADONE METHADONE HYDROCHLORIDE 5MG TABLET, EFFERVESCENT;ORAL Discontinued None No No
WESTADONE METHADONE HYDROCHLORIDE 10MG TABLET, EFFERVESCENT;ORAL Discontinued None No No
WESTADONE METHADONE HYDROCHLORIDE 40MG TABLET, EFFERVESCENT;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
03/14/1973 ORIG-1 Approval Type 3 - New Dosage Form STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
12/12/1979 SUPPL-8 Labeling

Label is not available on this site.

06/03/1977 SUPPL-7 Labeling

Label is not available on this site.

04/25/1977 SUPPL-5 Labeling

Label is not available on this site.

09/07/1976 SUPPL-3 Labeling

Label is not available on this site.

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