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FDA ANDA · ANDA073529

DOXAPRAM HYDROCHLORIDE

Sponsor: WATSON LABS

APPLICATION
ANDA073529
TYPE
ANDA
ORIGINAL APPROVAL
1992-01-30
LATEST ACTION
1999-02-19
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued

Products

DOXAPRAM HYDROCHLORIDEDiscontinued
DOXAPRAM HYDROCHLORIDE 20MG/ML · INJECTABLE · INJECTION

Approval history

1999-02-19Manufacturing (CMC) · Supplement 4AP
1999-02-02Manufacturing (CMC) · Supplement 2AP
1996-12-04Manufacturing (CMC) · Supplement 1AP
1992-01-30OriginalAP
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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