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FDA ANDA · ANDA070917

NALBUPHINE HYDROCHLORIDE

Sponsor: ABBOTT

APPLICATION
ANDA070917
TYPE
ANDA
ORIGINAL APPROVAL
1989-02-03
LATEST ACTION
1996-04-26
ROUTE
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
DOSAGE FORM
SOLUTION
MARKETING STATUS
Discontinued

Products

NALBUPHINE HYDROCHLORIDEDiscontinued
NALBUPHINE HYDROCHLORIDE 20MG/ML (20MG/ML) · SOLUTION · INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

Approval history

1996-04-26Labeling · Supplement 3AP
1991-02-28Labeling · Supplement 2AP
1990-07-25Labeling · Supplement 1AP
1989-02-03OriginalAP
VIEW ON DRUGS@FDA ↗

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