Succinylcholine Chloride 71839-0121-25

Package NDC

71839-0121-25

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]

Selected Package

71839-0121-25Selected

25 VIAL, MULTI-DOSE in 1 CARTON (71839-121-25) / 10 mL in 1 VIAL, MULTI-DOSE (71839-121-01)