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Succinylcholine Chloride

NDC 70518-4409 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA211589
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsSUCCINYLCHOLINE CHLORIDE (20 mg/mL)
Marketing started20250729
Package count1

External sources

Source: openFDA. Public-domain (CC0).