| NDC Code | 49580-0382-4 |
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| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (49580-0382-4) / 118 mL in 1 BOTTLE, PLASTIC |
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| Product NDC | 49580-0382 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Tussin Cf |
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| Proprietary Name Suffix | Multi Symptom Cold Adult |
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| Non-Proprietary Name | Dextromethorphan Hbr, Guaifenesin, Phenylephrine |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 20150430 |
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| End Marketing Date | 20250430 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | P & L Development, LLC |
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| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 20; 200; 10 |
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| Strength Unit | mg/10mL; mg/10mL; mg/10mL |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], 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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