Furosemide
NDC 42571-437, Furosemide, injection, from Micro Labs Limited.
- Product NDC
- 42571-437
- Status
- Listed
- Labeler
- Micro Labs Limited
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR, INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA218188
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42571-437 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FUROSEMIDE40 mg/4mL
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE]; Loop Diuretic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42571-437-66 | 42571043766 | 25 VIAL in 1 CARTON (42571-437-66) / 4 mL in 1 VIAL (42571-437-86) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2f547f7c-0322-465c-9764-43f955d98ab2
Use it
Look up 42571-437 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42571-437 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42571-437. 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.