| NDC Code | 71839-105-24 |
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| Package Description | 24 CARTON in 1 CARTON (71839-105-24) > 1 VIAL, MULTI-DOSE in 1 CARTON (71839-105-01) > 10 mL in 1 VIAL, MULTI-DOSE |
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| Product NDC | 71839-105 |
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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 |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20190513 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212512 |
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| Manufacturer | BE Pharmaceuticals Inc. |
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| Substance Name | NEOSTIGMINE METHYLSULFATE |
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| Strength | .5 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA] |
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