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FDA ANDA · ANDA074729

TOLMETIN SODIUM

Sponsor: COSETTE PHARMS NC

APPLICATION
ANDA074729
TYPE
ANDA
ORIGINAL APPROVAL
1997-02-27
LATEST ACTION
2024-11-21
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

TOLMETIN SODIUMDiscontinued
TOLMETIN SODIUM EQ 600MG BASE · TABLET · ORAL

Approval history

2024-11-21Labeling · Supplement 12 · standardAP
2021-04-28Labeling · Supplement 11 · standardAP
2016-05-09Labeling · Supplement 10 · standardAP
1999-12-02Manufacturing (CMC) · Supplement 8AP
1999-12-02Manufacturing (CMC) · Supplement 9AP
1999-02-12Manufacturing (CMC) · Supplement 1AP
1999-02-12Manufacturing (CMC) · Supplement 2AP
1997-02-27OriginalAP
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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