| NDC Code | 79739-7320-5 | 
|---|
			| Package Description | 500 TABLET in 1 BOTTLE (79739-7320-5) | 
|---|
			| Product NDC | 79739-7320 | 
|---|
			| 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 | 20181101 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA209587 | 
|---|
			| Manufacturer | LGM PHARMA SOLUTIONS, LLC | 
|---|
			| 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 | 
|---|