| NDC Code | 49884-235-37 |
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| Package Description | 115 mL in 1 BOTTLE (49884-235-37) |
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| Product NDC | 49884-235 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydrocodone Polistirex And Chlorpheniramine Polisitrex |
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| Non-Proprietary Name | Hydrocodone Polistirex And Chlorpheniramine Polisitrex |
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| Dosage Form | SUSPENSION, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20120816 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091632 |
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| Manufacturer | Par Pharmaceutical Companies Inc |
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| Substance Name | HYDROCODONE BITARTRATE; CHLORPHENIRAMINE MALEATE |
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| Strength | 10; 8 |
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| Strength Unit | mg/5mL; mg/5mL |
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| Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
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| DEA Schedule | CII |
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