# Anagrelide

NDC: 62135-313
Generic name: Anagrelide
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20050418

FDA application: ANDA076683

## Active ingredients

- ANAGRELIDE HYDROCHLORIDE ANHYDROUS: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62135-313"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-313
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e031dfb3-56e1-4fea-95f2-c2936e2057a0