| NDC Code | 17856-0301-1 |
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| Package Description | 72 CUP in 1 CASE (17856-0301-1) > 5 mL in 1 CUP |
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| Product NDC | 17856-0301 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydrocodone Polistirex And Chlorpheniramine Polistirex |
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| Non-Proprietary Name | Hydrocodone Polistirex And Chlorpheniramine Polistirex |
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| Dosage Form | SUSPENSION, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20141023 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091671 |
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| Manufacturer | Atlantic Biologicals Corps |
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| Substance Name | HYDROCODONE; CHLORPHENIRAMINE |
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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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