Butapap

Product NDC

46672-099

11-digit product format

466720099

Labeler code

46672

Product ID

46672-099_af879cb3-a37c-1397-e053-2995a90aa233

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

butalbital and acetaminophen

Dosage form

TABLET

Route

ORAL

Labeler

Mikart, LLC

Application

ANDA089987

Marketing category

ANDA

Marketing start

1992-10-26

Marketing end

0000-00-00

Substance

BUTALBITAL; ACETAMINOPHEN

Active strength

50 mg/1; mg/1

Pharmacologic classes

Barbiturates [CS],Barbiturate [EPC]

DEA schedule

CIII

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record