| NDC Code | 49999-151-20 |
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| Package Description | 20 TABLET in 1 BOTTLE, PLASTIC (49999-151-20) |
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| Product NDC | 49999-151 |
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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 | 20101011 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA088616 |
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| Manufacturer | Lake Erie Medical DBA Quality Care Products 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 | Barbiturates [CS],Barbiturate [EPC],Central Nervous System Stimulant [EPC],Methylxanthine [EPC],Xanthines [CS],Central Nervous System Stimulation [PE] |
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