Details for New Drug Application (NDA): 218878
The generic ingredient in SUCCINYLCHOLINE CHLORIDE is succinylcholine chloride. There is one drug master file entry for this compound. Twenty-eight suppliers are listed for this compound. Additional details are available on the succinylcholine chloride profile page.
Summary for 218878
| Tradename: | SUCCINYLCHOLINE CHLORIDE |
| Applicant: | Baxter Hlthcare Corp |
| Ingredient: | succinylcholine chloride |
| Patents: | 0 |
Pharmacology for NDA: 218878
| Physiological Effect | Neuromuscular Depolarizing Blockade |
Medical Subject Heading (MeSH) Categories for 218878
Suppliers and Packaging for NDA: 218878
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| SUCCINYLCHOLINE CHLORIDE | succinylcholine chloride | INJECTABLE;INJECTION | 218878 | ANDA | Baxter Healthcare Corporation | 43066-127 | 43066-127-05 | 5 CARTON in 1 CARTON (43066-127-05) / 1 SYRINGE, PLASTIC in 1 CARTON (43066-127-01) / 5 mL in 1 SYRINGE, PLASTIC |
| SUCCINYLCHOLINE CHLORIDE | succinylcholine chloride | INJECTABLE;INJECTION | 218878 | ANDA | Baxter Healthcare Corporation | 43066-129 | 43066-129-05 | 5 CARTON in 1 CARTON (43066-129-05) / 1 SYRINGE, PLASTIC in 1 CARTON (43066-129-01) / 10 mL in 1 SYRINGE, PLASTIC |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 20MG/ML | ||||
| Approval Date: | Sep 24, 2024 | TE: | AP | RLD: | No | ||||
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