Fioricet
- Product NDC
- 65084-454
- 11-digit product format
- 650840454
- Labeler code
- 65084
- Product ID
- 65084-454_c729a9da-6852-4500-89f8-047a42a43f99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Butalbital, Acetaminophen, and Caffeine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- McKesson Corporation dba RX Pak
- Application
- ANDA040885
- Marketing category
- ANDA
- Marketing start
- 2013-07-29
- Marketing end
- 0000-00-00
- Substance
- BUTALBITAL; ACETAMINOPHEN; CAFFEINE
- Active strength
- 50 mg/1; mg/1; mg/1
- Pharmacologic classes
- Barbiturates [CS],Barbiturate [EPC],Central Nervous System Stimulant [EPC],Methylxanthine [EPC],Xanthines [CS],Central Nervous System Stimulation [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record