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FDA ANDA · ANDA088267

DIETHYLPROPION HYDROCHLORIDE

Sponsor: CHARTWELL RX

APPLICATION
ANDA088267
TYPE
ANDA
ORIGINAL APPROVAL
1983-08-25
LATEST ACTION
2000-10-06
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

DIETHYLPROPION HYDROCHLORIDEDiscontinued
DIETHYLPROPION HYDROCHLORIDE 25MG · TABLET · ORAL

Approval history

2000-10-06Manufacturing (CMC) · Supplement 16AP
1991-01-31Labeling · Supplement 11AP
1989-05-01Labeling · Supplement 10AP
1989-04-20Manufacturing (CMC) · Supplement 7AP
1989-02-01Labeling · Supplement 8AP
1988-04-26Manufacturing (CMC) · Supplement 6AP
1983-12-16Manufacturing (CMC) · Supplement 2AP
1983-12-16Manufacturing (CMC) · Supplement 3AP
1983-11-29Manufacturing (CMC) · Supplement 1AP
1983-08-25OriginalAP
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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