Bumetanide
NDC 72205-057, Bumetanide, tablet, from Novadoz Pharmaceuticals LLC.
- Product NDC
- 72205-057
- Status
- Listed
- Labeler
- Novadoz Pharmaceuticals LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215362
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72205-057 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUMETANIDE1 mg/1
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE]; Loop Diuretic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72205-057-05 | 72205005705 | 500 TABLET in 1 BOTTLE (72205-057-05) |
| 72205-057-91 | 72205005791 | 100 TABLET in 1 BOTTLE (72205-057-91) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/cddd33fb-25b0-49ca-ab32-7c79a9b3a384
Use it
Look up 72205-057 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72205-057 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72205-057. 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.