# Granisetron Hydrochloride

NDC: 67457-863
Generic name: Granisetron Hydrochloride
Labeler / Manufacturer: Mylan Institutional LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20180321

FDA application: ANDA091136

## Active ingredients

- GRANISETRON HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67457-863"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67457-863
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8d88adba-7f5e-4e97-84b3-6ca8ec98c023