# Alosetron

NDC: 63629-2517
Generic name: Alosetron
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200914

FDA application: ANDA213614

## Active ingredients

- ALOSETRON HYDROCHLORIDE: .5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-2517"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-2517
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=da94d161-0bf0-48fe-90f4-8e38ae18e1ca