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FDA ANDA · ANDA071319

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Sponsor: SUPERPHARM

APPLICATION
ANDA071319
TYPE
ANDA
ORIGINAL APPROVAL
1987-01-06
LATEST ACTION
1988-11-03
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHENDiscontinued
ACETAMINOPHEN 650MG, PROPOXYPHENE NAPSYLATE 100MG · TABLET · ORAL

Approval history

1988-11-03Labeling · Supplement 3AP
1987-01-06OriginalAP
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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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