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