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FDA ANDA · ANDA087032

CHLORPROMAZINE HYDROCHLORIDE

Sponsor: WOCKHARDT

APPLICATION
ANDA087032
TYPE
ANDA
ORIGINAL APPROVAL
1982-07-08
LATEST ACTION
1990-03-30
ROUTE
ORAL
DOSAGE FORM
CONCENTRATE
MARKETING STATUS
Discontinued

Products

CHLORPROMAZINE HYDROCHLORIDEDiscontinued
CHLORPROMAZINE HYDROCHLORIDE 30MG/ML · CONCENTRATE · ORAL

Approval history

1990-03-30Labeling · Supplement 14AP
1989-11-30Labeling · Supplement 12AP
1989-06-21Labeling · Supplement 13AP
1988-07-28Manufacturing (CMC) · Supplement 10AP
1988-07-28Manufacturing (CMC) · Supplement 9AP
1988-07-28Manufacturing (CMC) · Supplement 11AP
1987-05-18Manufacturing (CMC) · Supplement 5AP
1985-08-07Manufacturing (CMC) · Supplement 3AP
1982-07-08OriginalAP
VIEW ON DRUGS@FDA ↗

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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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