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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 207834
Company: CHARTWELL
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
OXYCODONE AND ACETAMINOPHEN ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325MG;5MG TABLET;ORAL Discontinued None No No
OXYCODONE AND ACETAMINOPHEN ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325MG;7.5MG TABLET;ORAL Discontinued None No No
OXYCODONE AND ACETAMINOPHEN ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325MG;10MG 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
08/15/2019 ORIG-1 Approval 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
12/23/2025 SUPPL-5 Labeling-Package Insert, Labeling-Medication Guide

Label is not available on this site.

12/22/2025 SUPPL-4 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

03/27/2024 SUPPL-3 Labeling-Package Insert, Labeling-Medication Guide

Label is not available on this site.

01/02/2024 SUPPL-2 Labeling-Package Insert, Labeling-Medication Guide

Label is not available on this site.

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