# SUCCINYLCHOLINE CHLORIDE

NDC: 43066-129
Generic name: SUCCINYLCHOLINE CHLORIDE
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20240924

FDA application: ANDA218878

## Active ingredients

- SUCCINYLCHOLINE CHLORIDE DIHYDRATE: 20 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43066-129"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43066-129
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=30f58922-3c74-4813-ace0-fcd2024acd09