CHOLESTYRAMINE LIGHT
NDC 24658-270, cholestyramine light, powder, for suspension, from PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS.
- Product NDC
- 24658-270
- Status
- Listed
- Labeler
- PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA074558
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/24658-270 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CHOLESTYRAMINE4 g/5.7g
Pharmacologic classes
Bile Acid Sequestrant [EPC]; Bile-acid Binding Activity [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 24658-270-95 | 24658027095 | 60 POUCH in 1 CARTON (24658-270-95) / 5.7 g in 1 POUCH |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/31655681-125c-4eaa-959b-8f434bb43590NADAC price for package 24658027095
GET /v1/drugs/nadac/24658027095
Use it
Look up 24658-270 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/24658-270 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 24658-270. 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.