Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 077454
Company: ANI PHARMS

• REMS

Products on ANDA 077454

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
HYDROCODONE BITARTRATE AND IBUPROFEN	HYDROCODONE BITARTRATE; IBUPROFEN	5MG;200MG	TABLET;ORAL	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 077454

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
06/23/2010	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
10/02/2024	SUPPL-9	Labeling-Medication Guide, Labeling-Package Insert		Label is not available on this site.
12/15/2023	SUPPL-8	Labeling-Package Insert		Label is not available on this site.
04/28/2021	SUPPL-7	Labeling-Package Insert		Label is not available on this site.
03/04/2021	SUPPL-6	Labeling-Package Insert		Label is not available on this site.
10/11/2019	SUPPL-5	Labeling-Package Insert		Label is not available on this site.
07/22/2019	SUPPL-4	Labeling-Package Insert		Label is not available on this site.
09/18/2018	SUPPL-3	REMS - PROPOSAL - D-N-A		Label is not available on this site.
09/21/2018	SUPPL-2	Labeling-Package Insert, Labeling-Medication Guide		Label is not available on this site.
08/15/2018	SUPPL-1	Labeling-Package Insert, Labeling-Medication Guide		Label is not available on this site.