| NDC Code | 76045-214-30 |
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| Package Description | 10 BLISTER PACK in 1 CARTON (76045-214-30) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-214-00) / 3 mL in 1 SYRINGE, GLASS |
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| Product NDC | 76045-214 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Neostigmine Methylsulfate |
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| Non-Proprietary Name | Neostigmine Methylsulfate |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20180918 |
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| Marketing Category Name | NDA |
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| Application Number | NDA203629 |
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| Manufacturer | Fresenius Kabi USA, LLC |
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| Substance Name | NEOSTIGMINE METHYLSULFATE |
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| Strength | 1 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA] |
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