"54569-0339-4" National Drug Code (NDC)

NDC Code	54569-0339-4
Package Description	30 TABLET in 1 BOTTLE, PLASTIC (54569-0339-4)
Product NDC	54569-0339
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Butalbital, Aspirin And Caffeine
Non-Proprietary Name	Butalbital, Aspirin And Caffeine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19790605
Marketing Category Name	ANDA
Application Number	ANDA086162
Manufacturer	A-S Medication Solutions LLC
Substance Name	BUTALBITAL; ASPIRIN; CAFFEINE
Strength	50; 325; 40
Strength Unit	mg/1; mg/1; mg/1
Pharmacy Classes	Barbiturate [EPC],Barbiturates [Chemical/Ingredient],Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Platelet Aggregation Inhibitor [EPC],Decreased Platelet Aggregation [PE],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient]
DEA Schedule	CIII