Prednisone
NDC 42708-105, Prednisone, tablet, from QPharma, Inc..
- Product NDC
- 42708-105
- Status
- Listed
- Labeler
- QPharma, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA085161
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42708-105 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PREDNISONE20 mg/1
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42708-105-10 | 42708010510 | 10 TABLET in 1 BOTTLE (42708-105-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/d898d53f-c7d2-4bdb-bd9e-5f200070d123
Use it
Look up 42708-105 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42708-105 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42708-105. 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.