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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 085513
Company: ABBOTT
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
A-POXIDE CHLORDIAZEPOXIDE HYDROCHLORIDE 25MG CAPSULE;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
06/30/1977 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
01/25/1984 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

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