Flunisolide
NDC 50742-317, Flunisolide, solution, from Ingenus Pharmaceuticals, LLC.
- Product NDC
- 50742-317
- Status
- Listed
- Labeler
- Ingenus Pharmaceuticals, LLC
- Dosage form
- SOLUTION
- Route
- NASAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207802
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50742-317 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUNISOLIDE.25 mg/mL
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50742-317-25 | 50742031725 | 1 BOTTLE, PUMP in 1 CARTON (50742-317-25) / 25 mL in 1 BOTTLE, PUMP |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/f39cae46-c68f-47ef-82f3-4fd3dd46c74cNADAC price for package 50742031725
GET /v1/drugs/nadac/50742031725
Use it
Look up 50742-317 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50742-317 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50742-317. 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.