NDC Code | 50090-7042-3 |
Package Description | 100 TABLET in 1 BOTTLE (50090-7042-3) |
Product NDC | 50090-7042 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Butalbital, Acetaminophen, Caffeine |
Non-Proprietary Name | Butalbital, Acetaminophen, And Caffeine |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20190305 |
Marketing Category Name | ANDA |
Application Number | ANDA209587 |
Manufacturer | A-S Medication Solutions |
Substance Name | ACETAMINOPHEN; BUTALBITAL; CAFFEINE |
Strength | 325; 50; 40 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmacy Classes | Barbiturate [EPC], Barbiturates [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS] |
DEA Schedule | CIII |