| NDC Code | 66689-004-50 |
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| Package Description | 50 CUP, UNIT-DOSE in 1 CASE (66689-004-50) / 5 mL in 1 CUP, UNIT-DOSE (66689-004-01) |
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| Product NDC | 66689-004 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
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| Non-Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20190624 |
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| End Marketing Date | 20241130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200343 |
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| Manufacturer | VistaPharm, LLC |
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| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
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| Strength | 108; 2.5 |
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| Strength Unit | mg/5mL; mg/5mL |
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| Pharmacy Classes | Opioid Agonist [EPC], Opioid Agonists [MoA] |
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| DEA Schedule | CII |
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