Cholestyramine
NDC 51224-011, Cholestyramine, powder, for suspension, from TAGI Pharma, Inc..
- Product NDC
- 51224-011
- Status
- Listed
- Labeler
- TAGI Pharma, Inc.
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209597
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51224-011 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CHOLESTYRAMINE4 g/8.3g
Pharmacologic classes
Bile Acid Sequestrant [EPC]; Bile-acid Binding Activity [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51224-011-10 | 51224001110 | 348.6 g in 1 CAN (51224-011-10) |
| 51224-011-20 | 51224001120 | 60 POUCH in 1 CARTON (51224-011-20) / 8.3 g in 1 POUCH |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/06261db5-1435-4b91-8b54-71bfcfb1368c
Use it
Look up 51224-011 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51224-011 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51224-011. 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.