United States · FDA National Drug Code directory
Colestipol Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50742-284_f784d09d-69b6-4e7b-a1eb-8b7e839cd4db
- Product NDC
- 50742-284
- Form
- TABLET, FILM COATED
- Composition / generic term
- Colestipol Hydrochloride
- Labeler
- Ingenus Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241203
- Source listing expiry
- 20261231
Source-listed ingredients
- COLESTIPOL HYDROCHLORIDE — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET, FILM COATED in 1 BOTTLE (50742-284-12) · 50742-284-12
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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