| NDC Code | 0722-7320-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (0722-7320-05) |
|---|
| Product NDC | 0722-7320 |
|---|
| 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 | Nexgen Pharma, Inc. |
|---|
| Substance Name | BUTALBITAL; ACETAMINOPHEN; CAFFEINE |
|---|
| Strength | 50; 325; 40 |
|---|
| Strength Unit | mg/1; mg/1; mg/1 |
|---|
| Pharmacy Classes | Barbiturates [CS],Barbiturate [EPC],Central Nervous System Stimulant [EPC],Methylxanthine [EPC],Xanthines [CS],Central Nervous System Stimulation [PE] |
|---|
| DEA Schedule | CIII |
|---|