Details for New Drug Application (NDA): 217808
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NDA 217808 describes SUCCINYLCHOLINE CHLORIDE, which is a drug marketed by Accord Hlthcare, Adaptis, Amneal, Amphastar Pharms Inc, Amring Pharms, Aspiro, Baxter Hlthcare Corp, Be Pharms, Breckenridge, Deva Holding As, Dr Reddys, Eugia Pharma, Fresenius Kabi Usa, Gland Pharma Ltd, Hikma, Intl Medication, Mankind Pharma, Meitheal, Micro Labs, Nexus, Organon Usa Inc, Sagent Pharms Inc, Somerset Theraps Llc, Umedica, Zydus Pharms, and Steriscience, and is included in twenty-eight NDAs. It is available from twenty-five suppliers. Additional details are available on the SUCCINYLCHOLINE CHLORIDE profile page.
The generic ingredient in SUCCINYLCHOLINE CHLORIDE is succinylcholine chloride. There are six drug master file entries for this compound. Twenty-nine suppliers are listed for this compound. Additional details are available on the succinylcholine chloride profile page.
The generic ingredient in SUCCINYLCHOLINE CHLORIDE is succinylcholine chloride. There are six drug master file entries for this compound. Twenty-nine suppliers are listed for this compound. Additional details are available on the succinylcholine chloride profile page.
Summary for 217808
| Tradename: | SUCCINYLCHOLINE CHLORIDE |
| Applicant: | Eugia Pharma |
| Ingredient: | succinylcholine chloride |
| Patents: | 0 |
Pharmacology for NDA: 217808
| Physiological Effect | Neuromuscular Depolarizing Blockade |
Medical Subject Heading (MeSH) Categories for 217808
Suppliers and Packaging for NDA: 217808
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| SUCCINYLCHOLINE CHLORIDE | succinylcholine chloride | INJECTABLE;INJECTION | 217808 | ANDA | Eugia US LLC | 55150-315 | 55150-315-25 | 25 VIAL, MULTI-DOSE in 1 CARTON (55150-315-25) / 10 mL in 1 VIAL, MULTI-DOSE (55150-315-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 20MG/ML | ||||
| Approval Date: | Oct 16, 2023 | TE: | RLD: | No | |||||
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