| NDC Code | 21130-959-06 |
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| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (21130-959-06) / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
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| Product NDC | 21130-959 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Pain Relief |
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| Proprietary Name Suffix | Added Strength |
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| Non-Proprietary Name | Acetaminophen, Aspirin, Caffeine |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 19921117 |
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| End Marketing Date | 20241222 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M013 |
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| Manufacturer | Better Living Brands, LLC |
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| Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
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| Strength | 250; 250; 65 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS] |
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