Bumetanide
NDC 31722-368, Bumetanide, injection, from Camber Pharmaceuticals, Inc..
- Product NDC
- 31722-368
- Status
- Listed
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR, INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA218746
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/31722-368 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUMETANIDE.25 mg/mL
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE]; Loop Diuretic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 31722-368-32 | 31722036832 | 10 VIAL, SINGLE-DOSE in 1 CARTON (31722-368-32) / 4 mL in 1 VIAL, SINGLE-DOSE (31722-368-31) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/084b34ad-36ba-43bd-a43a-1f4b4da26d8f
Use it
Look up 31722-368 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/31722-368 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 31722-368. 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.