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FDA ANDA · ANDA074106

NAPROXEN SODIUM

Sponsor: HAMILTON PHARMS

APPLICATION
ANDA074106
TYPE
ANDA
ORIGINAL APPROVAL
1993-08-31
LATEST ACTION
1995-12-28
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

NAPROXEN SODIUMDiscontinued
NAPROXEN SODIUM EQ 250MG BASE · TABLET · ORAL
NAPROXEN SODIUMDiscontinued
NAPROXEN SODIUM EQ 500MG BASE · TABLET · ORAL

Approval history

1995-12-28Labeling · Supplement 1AP
1993-08-31OriginalAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industry →GMP discipline →FDA drug shortages →FDA enforcement & recalls →

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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