| NDC Code | 68084-396-65 | 
|---|
			| Package Description | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-396-65)  > 1 TABLET in 1 BLISTER PACK (68084-396-11) | 
|---|
			| Product NDC | 68084-396 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Butalbital, Acetaminophen And Caffeine | 
|---|
			
			| Non-Proprietary Name | Butalbital, Acetaminophen And Caffeine | 
|---|
			| Dosage Form | TABLET | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20090908 | 
|---|
			| End Marketing Date | 20240331 | 
|---|
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA040511 | 
|---|
			| Manufacturer | American Health Packaging | 
|---|
			| 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 | 
|---|