Butisol Sodium

Product NDC

0037-0113

11-digit product format

000370113

Labeler code

0037

Product ID

0037-0113_0e16e8e0-efa1-43df-aba4-2e3cad8af753

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Butabarbital Sodium

Dosage form

TABLET

Route

ORAL

Labeler

Meda Pharmaceuticals

Application

NDA000793

Marketing category

NDA

Marketing start

1939-08-01

Marketing end

2020-01-31

Substance

BUTABARBITAL SODIUM

Active strength

30 mg/1

DEA schedule

CIII

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record