prednisone
NDC 42708-186, PREDNISONE, tablet, from QPharma Inc.
- Product NDC
- 42708-186
- Status
- Listed
- Labeler
- QPharma Inc
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208412
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42708-186 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PREDNISONE5 mg/1
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42708-186-21 | 42708018621 | 21 TABLET in 1 BOTTLE, PLASTIC (42708-186-21) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/11870c93-fe64-e6c9-e063-6394a90a5334
Use it
Look up 42708-186 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42708-186 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42708-186. 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.