Cholestyramine Light
NDC 51224-009, Cholestyramine, powder, for suspension, from TAGI Pharma, Inc..
- Product NDC
- 51224-009
- Status
- Listed
- Labeler
- TAGI Pharma, Inc.
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209599
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51224-009 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CHOLESTYRAMINE4 g/4.8g
Pharmacologic classes
Bile Acid Sequestrant [EPC]; Bile-acid Binding Activity [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51224-009-10 | 51224000910 | 201.6 g in 1 CAN (51224-009-10) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/eb85a2c8-cdc3-48bb-844d-e220ae3701a0
Use it
Look up 51224-009 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51224-009 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51224-009. 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.