Difluprednate Ophthalmic
NDC 0781-6000, Difluprednate Ophthalmic, emulsion, from Sandoz Inc.
- Product NDC
- 0781-6000
- Status
- Listed
- Labeler
- Sandoz Inc
- Dosage form
- EMULSION
- Route
- OPHTHALMIC
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA022212
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0781-6000 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DIFLUPREDNATE.5 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0781-6000-78 | 00781600078 | 1 BOTTLE in 1 CARTON (0781-6000-78) / 5 mL in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/0f60b857-7898-4a9e-935c-a9ddf0eb9194NADAC price for package 00781600078
GET /v1/drugs/nadac/00781600078
Use it
Look up 0781-6000 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0781-6000 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0781-6000. 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.