# vecuronium bromide

NDC: 47335-932
Generic name: vecuronium bromide
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20141215

FDA application: ANDA079001

## Active ingredients

- VECURONIUM BROMIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-932"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-932
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a14da3ee-a731-4282-be9d-407473517470