# Rocuronium Bromide

NDC: 71288-718
Generic name: Rocuronium Bromide
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20230508

FDA application: ANDA213453

## Active ingredients

- ROCURONIUM BROMIDE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-718"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-718
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b9abaf64-760d-43e0-8669-a9ca70feab11