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FDA ANDA · ANDA083278

PROPOXYPHENE HYDROCHLORIDE

Sponsor: PUREPAC PHARM

APPLICATION
ANDA083278
TYPE
ANDA
ORIGINAL APPROVAL
1973-01-15
LATEST ACTION
1988-05-09
ROUTE
ORAL
DOSAGE FORM
CAPSULE
MARKETING STATUS
Discontinued

Products

PROPOXYPHENE HYDROCHLORIDEDiscontinued
PROPOXYPHENE HYDROCHLORIDE 65MG · CAPSULE · ORAL

Approval history

1988-05-09Labeling · Supplement 28AP
1973-01-15OriginalAP
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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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