| NDC Code | 46672-059-50 |
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| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (46672-059-50) |
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| Product NDC | 46672-059 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Butalbital, Acetaminophen And Caffeine |
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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 | 19880523 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA089451 |
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| Manufacturer | Mikart, Inc. |
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| Substance Name | ACETAMINOPHEN; BUTALBITAL; CAFFEINE |
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| Strength | 500; 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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