Bumetanide
NDC 60687-535, Bumetanide, tablet, from American Health Packaging.
- Product NDC
- 60687-535
- Status
- Listed
- Labeler
- American Health Packaging
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA018225
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/60687-535 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUMETANIDE2 mg/1
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE]; Loop Diuretic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60687-535-65 | 60687053565 | 50 BLISTER PACK in 1 CARTON (60687-535-65) / 1 TABLET in 1 BLISTER PACK (60687-535-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5e9633e4-151b-4f40-885e-8f364f6f2d18NADAC price for package 60687053565
GET /v1/drugs/nadac/60687053565
Use it
Look up 60687-535 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60687-535 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60687-535. 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.