Colestipol Hydrochloride
NDC 50742-284, Colestipol Hydrochloride, tablet, film coated, from Ingenus Pharmaceuticals, LLC.
- Product NDC
- 50742-284
- Status
- Listed
- Labeler
- Ingenus Pharmaceuticals, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217462
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50742-284 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- COLESTIPOL HYDROCHLORIDE1 g/1
Pharmacologic classes
Bile Acid Sequestrant [EPC]; Bile-acid Binding Activity [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50742-284-12 | 50742028412 | 120 TABLET, FILM COATED in 1 BOTTLE (50742-284-12) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3fa27483-8346-4145-81c0-5527204d7d68NADAC price for package 50742028412
GET /v1/drugs/nadac/50742028412
Use it
Look up 50742-284 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50742-284 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50742-284. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.