| NDC Code | 0409-2051-05 |
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| Package Description | 10 VIAL, MULTI-DOSE in 1 BOX (0409-2051-05) / 5 mL in 1 VIAL, MULTI-DOSE (0409-2051-15) |
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| Product NDC | 0409-2051 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ketamine Hydrochloride |
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| Non-Proprietary Name | Ketamine Hydrochloride |
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| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20041130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074549 |
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| Manufacturer | Hospira, Inc. |
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| Substance Name | KETAMINE HYDROCHLORIDE |
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| Strength | 100 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | General Anesthesia [PE], General Anesthetic [EPC] |
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| DEA Schedule | CIII |
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