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FDA ANDA · ANDA213195

NALTREXONE

Sponsor: TEVA PHARMS USA INC

APPLICATION
ANDA213195
TYPE
ANDA
ORIGINAL APPROVAL
2023-07-06
LATEST ACTION
2023-07-06
ROUTE
INTRAMUSCULAR
DOSAGE FORM
FOR SUSPENSION, EXTENDED RELEASE
MARKETING STATUS
Discontinued

Products

NALTREXONEDiscontinued
NALTREXONE 380MG/VIAL · FOR SUSPENSION, EXTENDED RELEASE · INTRAMUSCULAR

Approval history

2023-07-06UNKNOWN · Original · standardLetterAP
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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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