PredniSONE Tablets, USP, 10 mg
NDC 63561-0121, PredniSONE, tablet, from Granulation Technology, Inc..
- Product NDC
- 63561-0121
- Status
- Listed
- Labeler
- Granulation Technology, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212629
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0121 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PREDNISONE10 mg/1
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 63561-0121-1 | 63561012101 | 100 TABLET in 1 BOTTLE (63561-0121-1) |
| 63561-0121-2 | 63561012102 | 1000 TABLET in 1 BOTTLE (63561-0121-2) |
| 63561-0121-5 | 63561012105 | 500 TABLET in 1 BOTTLE (63561-0121-5) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/a173fcbb-99be-4b3e-a3a4-4e9ae04ad83fNADAC price for package 63561012101
GET /v1/drugs/nadac/63561012101NADAC price for package 63561012102
GET /v1/drugs/nadac/63561012102NADAC price for package 63561012105
GET /v1/drugs/nadac/63561012105
Use it
Look up 63561-0121 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0121 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63561-0121. 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.