| NDC Code | 52544-957-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (52544-957-05) |
|---|
| Product NDC | 52544-957 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Fioricet |
|---|
| Non-Proprietary Name | Butalbital, Acetaminophen, And Caffeine |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19841109 |
|---|
| End Marketing Date | 20161130 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA088616 |
|---|
| Manufacturer | Watson Pharma, Inc. |
|---|
| Substance Name | ACETAMINOPHEN; BUTALBITAL; CAFFEINE |
|---|
| Strength | 325; 50; 40 |
|---|
| Strength Unit | mg/1; mg/1; mg/1 |
|---|
| Pharmacy Classes | Barbiturate [EPC],Barbiturates [Chemical/Ingredient],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |
|---|