# Colestipol Hydrochloride

NDC: 42799-115
Generic name: Colestipol Hydrochloride
Labeler / Manufacturer: Edenbridge Pharmaceuticals LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20241126

FDA application: ANDA217667

## Active ingredients

- COLESTIPOL HYDROCHLORIDE: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42799-115"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42799-115
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=03ca5800-4211-4383-a332-be88bd9b5304