Furosemide
NDC 63561-0164, FUROSEMIDE, tablet, from Granulation Technology, Inc..
- Product NDC
- 63561-0164
- Status
- Listed
- Labeler
- Granulation Technology, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA018569
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0164 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FUROSEMIDE20 mg/1
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE]; Loop Diuretic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 63561-0164-1 | 63561016401 | 100 TABLET in 1 BOTTLE (63561-0164-1) |
| 63561-0164-2 | 63561016402 | 1000 TABLET in 1 BOTTLE (63561-0164-2) |
| 63561-0164-9 | 63561016409 | 90 TABLET in 1 BOTTLE (63561-0164-9) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/462e8917-cbe0-f4f9-e063-6394a90ab4ffNADAC price for package 63561016402
GET /v1/drugs/nadac/63561016402
Use it
Look up 63561-0164 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0164 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63561-0164. 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.