| NDC Code | 52544-957-01 |
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| Package Description | 100 TABLET in 1 BOTTLE (52544-957-01) |
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| Product NDC | 52544-957 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Fioricet |
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| Non-Proprietary Name | Butalbital, Acetaminophen, And Caffeine |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 19841109 |
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| End Marketing Date | 20161130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA088616 |
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| Manufacturer | Watson Pharma, Inc. |
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| Substance Name | ACETAMINOPHEN; BUTALBITAL; CAFFEINE |
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| Strength | 325; 50; 40 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Barbiturate [EPC],Barbiturates [Chemical/Ingredient],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |
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