| NDC Code | 52682-041-03 |
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| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (52682-041-03) |
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| Product NDC | 52682-041 |
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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 | 20110808 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040864 |
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| Manufacturer | Mirror Pharmaceuticals LLC |
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| Substance Name | BUTALBITAL; ACETAMINOPHEN; CAFFEINE |
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| Strength | 50; 325; 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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