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FDA ANDA · ANDA084272

BUTABARBITAL SODIUM

Sponsor: SANDOZ

APPLICATION
ANDA084272
TYPE
ANDA
LATEST ACTION
1985-08-16
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

BUTABARBITAL SODIUMDiscontinued
BUTABARBITAL SODIUM 30MG · TABLET · ORAL

Approval history

1985-08-16Manufacturing (CMC) · Supplement 75AP
1984-06-05Manufacturing (CMC) · Supplement 73AP
1984-06-05Manufacturing (CMC) · Supplement 72AP
1983-07-26Manufacturing (CMC) · Supplement 71AP
1983-07-26Manufacturing (CMC) · Supplement 70AP
1983-05-16Manufacturing (CMC) · Supplement 69AP
1983-05-05Manufacturing (CMC) · Supplement 67AP
1982-11-26Manufacturing (CMC) · Supplement 66AP
1981-12-22Manufacturing (CMC) · Supplement 63AP
1981-12-22Manufacturing (CMC) · Supplement 61AP
1981-12-22Manufacturing (CMC) · Supplement 62AP
1981-12-22Manufacturing (CMC) · Supplement 60AP
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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