| NDC Code | 46122-700-71 |
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| Package Description | 1 BOTTLE in 1 CARTON (46122-700-71) / 50 TABLET in 1 BOTTLE |
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| Product NDC | 46122-700 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Gnp Mucus Relief |
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| Proprietary Name Suffix | Pe |
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| Non-Proprietary Name | Guaifenesin/phenylephrine |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20220113 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | AmerisourceBergen Drug Corp |
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| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 400; 10 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-1 Adrenergic Agonist [EPC] |
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