# Colestipol Hydrochloride

NDC: 50742-284
Generic name: Colestipol Hydrochloride
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20241203

FDA application: ANDA217462

## Active ingredients

- COLESTIPOL HYDROCHLORIDE: 1 g/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-284"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-284
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3fa27483-8346-4145-81c0-5527204d7d68