| NDC Code | 48201-001-12 |
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| Package Description | 12 CAPSULE, GELATIN COATED in 1 BOX (48201-001-12) |
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| Product NDC | 48201-001 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Sanaflu Xtra |
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| Non-Proprietary Name | Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |
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| Dosage Form | CAPSULE, GELATIN COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20150430 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M013 |
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| Manufacturer | GRANDALL DISTRIBUTING, LLC |
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| Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 250; 2; 10; 5 |
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| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
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