NDC Code | 70069-805-10 |
Package Description | 10 VIAL, MULTI-DOSE in 1 CARTON (70069-805-10) > 10 mL in 1 VIAL, MULTI-DOSE (70069-805-01) |
Product NDC | 70069-805 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Neostigmine Methylsulfate |
Non-Proprietary Name | Neostigmine Methylsulfate |
Dosage Form | INJECTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20220110 |
Marketing Category Name | ANDA |
Application Number | ANDA213074 |
Manufacturer | Somerset Therapeutics, LLC |
Substance Name | NEOSTIGMINE METHYLSULFATE |
Strength | .5 |
Strength Unit | mg/mL |
Pharmacy Classes | Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA] |