Butalbital And Acetaminophen

Product NDC
54879-026
11-digit product format
548790026
Labeler code
54879
Product ID
54879-026_9d6d119e-f188-4582-bdbd-b5f3949c9c83
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
butalbital and acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
STI Pharma LLC
Application
ANDA203484
Marketing category
ANDA
Marketing start
2016-11-15
Marketing end
0000-00-00
Substance
BUTALBITAL; ACETAMINOPHEN
Active strength
50 mg/1; mg/1
Pharmacologic classes
Barbiturates [CS],Barbiturate [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
54879-026-01EA - Each54879-02610c455db-1ee1-4436-84f1-6ee1a2d21c8912017-03-06