Prednisolone Sodium Phosphate
NDC 42799-812, Prednisolone Sodium Phosphate, solution, from Edenbridge Pharmaceuticals LLC..
- Product NDC
- 42799-812
- Status
- Listed
- Labeler
- Edenbridge Pharmaceuticals LLC.
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA203559
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42799-812 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PREDNISOLONE SODIUM PHOSPHATE10 mg/5mL
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42799-812-01 | 42799081201 | 237 mL in 1 BOTTLE, PLASTIC (42799-812-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/1793e218-7b49-497d-879f-1020de6e6d68NADAC price for package 42799081201
GET /v1/drugs/nadac/42799081201
Use it
Look up 42799-812 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42799-812 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42799-812. 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.