Details for New Drug Application (NDA): 218993
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The generic ingredient in MIDAZOLAM IN 0.9% SODIUM CHLORIDE is midazolam. There are nine drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the midazolam profile page.
Summary for 218993
Tradename: | MIDAZOLAM IN 0.9% SODIUM CHLORIDE |
Applicant: | Gland Pharma Ltd |
Ingredient: | midazolam |
Patents: | 0 |
Suppliers and Packaging for NDA: 218993
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
MIDAZOLAM IN 0.9% SODIUM CHLORIDE | midazolam | SOLUTION;INTRAVENOUS | 218993 | ANDA | Gland Pharma Limited | 68083-618 | 68083-618-10 | 10 POUCH in 1 CARTON (68083-618-10) / 1 BAG in 1 POUCH / 50 mL in 1 BAG |
MIDAZOLAM IN 0.9% SODIUM CHLORIDE | midazolam | SOLUTION;INTRAVENOUS | 218993 | ANDA | Gland Pharma Limited | 68083-619 | 68083-619-10 | 10 POUCH in 1 CARTON (68083-619-10) / 1 BAG in 1 POUCH / 100 mL in 1 BAG |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 50MG/50ML (1MG/ML) | ||||
Approval Date: | Aug 12, 2024 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 100MG/100ML (1MG/ML) | ||||
Approval Date: | Aug 12, 2024 | TE: | AP | RLD: | No |
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