| NDC Code | 68475-507-02 |
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| Package Description | 10 VIAL in 1 CARTON (68475-507-02) > 10 mL in 1 VIAL |
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| Product NDC | 68475-507 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Remifentanil Hydrochloride |
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| Non-Proprietary Name | Remifentanil Hydrochloride |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20210101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210594 |
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| Manufacturer | Navinta LLC |
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| Substance Name | REMIFENTANIL HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
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| DEA Schedule | CII |
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