| NDC Code | 50991-529-16 |
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| Package Description | 473 mL in 1 BOTTLE (50991-529-16) |
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| Product NDC | 50991-529 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Poly-tussin |
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| Proprietary Name Suffix | Ex |
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| Non-Proprietary Name | Dihydrocodeine Bitartrate, Phenylephrine Hydrochloride, And Guaifenesin |
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| Dosage Form | SYRUP |
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| Usage | ORAL |
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| Start Marketing Date | 20091116 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | Poly Pharmaceuticals, Inc. |
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| Substance Name | DIHYDROCODEINE BITARTRATE; PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN |
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| Strength | 7.5; 5; 50 |
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| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
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| Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC],alpha-1 Adrenergic Agonist [EPC],Adrenergic alpha1-Agonists [MoA] |
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| DEA Schedule | CIII |
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