# Anectine

NDC: 0781-9053
Generic name: Succinylcholine Chloride
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS, PARENTERAL
Marketing started: 20190612

FDA application: NDA008453

## Active ingredients

- SUCCINYLCHOLINE CHLORIDE: 20 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-9053"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-9053
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=04a4e6f5-6fa1-42e1-a3f9-21fca7786b15