Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 213195
Company: TEVA PHARMS USA INC

Products on ANDA 213195

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
NALTREXONE	NALTREXONE	380MG/VIAL	FOR SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 213195

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
07/06/2023	ORIG-1	Approval		STANDARD	Letter (PDF)	Label is not available on this site.	https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/213195Orig1s000ltr.pdf