# Granisol

NDC: 80056-801
Generic name: granisetron hydrochloride
Labeler / Manufacturer: Intra-Sana Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20250704

FDA application: ANDA219282

## Active ingredients

- GRANISETRON HYDROCHLORIDE: 2 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80056-801"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80056-801
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2758eb4d-2fe0-4f74-b3f5-b4903009e97c