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Furosemide

NDC 70121-1164, Furosemide, injection, from Amneal Pharmaceuticals LLC.

Product NDC
70121-1164
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207552
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70121-1164 \
  -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 NDCNDC-11Package
70121-1164-57012111640525 VIAL, GLASS in 1 CARTON (70121-1164-5) / 4 mL in 1 VIAL, GLASS (70121-1164-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d5b9f12e-d1e9-42de-90f2-c9ba33a86457

Use it

Look up 70121-1164 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70121-1164 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70121-1164. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.