PREDNISOLONE
NDC 60722-5011, PREDNISOLONE, tablet, from Zhejiang Xianju Pharmaceutical Co., Ltd..
- Product NDC
- 60722-5011
- Status
- Listed
- Labeler
- Zhejiang Xianju Pharmaceutical Co., Ltd.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA218083
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/60722-5011 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PREDNISOLONE5 mg/1
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60722-5011-0 | 60722501100 | 100 TABLET in 1 BOTTLE (60722-5011-0) |
| 60722-5011-1 | 60722501101 | 1000 TABLET in 1 BOTTLE (60722-5011-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/52e6e21d-94b8-41a0-8d13-371c0e66bcee
Use it
Look up 60722-5011 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60722-5011 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60722-5011. 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.