| NDC Code | 17856-0087-3 |
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| Package Description | 5 BOX, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0087-3) > 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0087-1) > 5 mL in 1 CUP, UNIT-DOSE |
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| Product NDC | 17856-0087 |
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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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| Proprietary Name Suffix | Extended-release |
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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 | 20150306 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091632 |
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| Manufacturer | ATLANTIC BIOLOGICALS CORP. |
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| Substance Name | CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE |
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| Strength | 8; 10 |
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| Strength Unit | mg/5mL; mg/5mL |
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| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Opioid Agonist [EPC], Opioid Agonists [MoA] |
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| DEA Schedule | CII |
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