Succinylcholine Chloride 71839-0121
Product NDC
71839-0121- Manufacturer
- Be Pharmaceuticals Inc.
- Dosage Form
- Injection, Solution
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- February 7, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA216003
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Succinylcholine Chloride | 20 mg/mL |
Drug Class
Depolarizing Neuromuscular Blocker [EPC]Neuromuscular Depolarizing Blockade [PE]
Packaging Options(1)
25 VIAL, MULTI-DOSE in 1 CARTON (71839-121-25) / 10 mL in 1 VIAL, MULTI-DOSE (71839-121-01)