Furosemide
NDC 17856-3298, Furosemide, solution, from Atlantic Biologicals Corps.
- Product NDC
- 17856-3298
- Status
- Listed
- Labeler
- Atlantic Biologicals Corps
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA070433
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/17856-3298 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FUROSEMIDE40 mg/5mL
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE]; Loop Diuretic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 17856-3298-1 | 17856329801 | 5 mL in 1 CUP (17856-3298-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9c342198-7162-4cc5-bda1-bc4054a4292b
Use it
Look up 17856-3298 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/17856-3298 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 17856-3298. 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.