Details for New Drug Application (NDA): 212968
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The generic ingredient in NEOSTIGMINE METHYLSULFATE is neostigmine methylsulfate. There are nine drug master file entries for this compound. Twenty-five suppliers are listed for this compound. Additional details are available on the neostigmine methylsulfate profile page.
Summary for 212968
Tradename: | NEOSTIGMINE METHYLSULFATE |
Applicant: | Gland Pharma Ltd |
Ingredient: | neostigmine methylsulfate |
Patents: | 0 |
Pharmacology for NDA: 212968
Mechanism of Action | Cholinesterase Inhibitors |
Medical Subject Heading (MeSH) Categories for 212968
Suppliers and Packaging for NDA: 212968
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
NEOSTIGMINE METHYLSULFATE | neostigmine methylsulfate | SOLUTION;INTRAVENOUS | 212968 | ANDA | Gland Pharma Limited | 68083-383 | 68083-383-10 | 10 CARTON in 1 CARTON (68083-383-10) / 1 VIAL, MULTI-DOSE in 1 CARTON (68083-383-01) / 10 mL in 1 VIAL, MULTI-DOSE |
NEOSTIGMINE METHYLSULFATE | neostigmine methylsulfate | SOLUTION;INTRAVENOUS | 212968 | ANDA | Gland Pharma Limited | 68083-384 | 68083-384-10 | 10 CARTON in 1 CARTON (68083-384-10) / 1 VIAL, MULTI-DOSE in 1 CARTON (68083-384-01) / 10 mL in 1 VIAL, MULTI-DOSE |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 5MG/10ML (0.5MG/ML) | ||||
Approval Date: | Oct 16, 2019 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 10MG/10ML (1MG/ML) | ||||
Approval Date: | Oct 16, 2019 | TE: | AP | RLD: | No |
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