prednisolone acetate
NDC 60219-2550, prednisolone acetate, suspension/ drops, from Amneal Pharmaceuticals NY LLC.
- Product NDC
- 60219-2550
- Status
- Listed
- Labeler
- Amneal Pharmaceuticals NY LLC
- Dosage form
- SUSPENSION/ DROPS
- Route
- OPHTHALMIC
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA218256
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/60219-2550 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PREDNISOLONE ACETATE10 mg/mL
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60219-2550-1 | 60219255001 | 1 BOTTLE, PLASTIC in 1 CARTON (60219-2550-1) / 5 mL in 1 BOTTLE, PLASTIC |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/8d8e8f9b-4d65-426f-8c57-451001cdd849NADAC price for package 60219255001
GET /v1/drugs/nadac/60219255001
Use it
Look up 60219-2550 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60219-2550 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60219-2550. 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.