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FDA ANDA · ANDA074402

CIMETIDINE

Sponsor: IVAX SUB TEVA PHARMS

APPLICATION
ANDA074402
TYPE
ANDA
ORIGINAL APPROVAL
1995-05-30
LATEST ACTION
1999-08-18
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

CIMETIDINEDiscontinued
CIMETIDINE 800MG · TABLET · ORAL

Approval history

1999-08-18Manufacturing (CMC) · Supplement 4AP
1997-05-30Manufacturing (CMC) · Supplement 3AP
1996-08-27Manufacturing (CMC) · Supplement 1AP
1996-08-27Manufacturing (CMC) · Supplement 2AP
1995-05-30OriginalAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

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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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