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Furosemide

NDC 83980-002, Furosemide, tablet, from Ipca Laboratories Limited.

Product NDC
83980-002
Status
Listed
Labeler
Ipca Laboratories Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078010
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/83980-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE20 mg/1

Pharmacologic classes

Increased Diuresis at Loop of Henle [PE]; Loop Diuretic [EPC]

Package NDCNDC-11Package
83980-002-0183980000201100 TABLET in 1 BOTTLE (83980-002-01)
83980-002-10839800002101000 TABLET in 1 BOTTLE (83980-002-10)
83980-002-978398000029710 TABLET in 1 BOTTLE (83980-002-97)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0acd293b-ecab-4879-a8e7-cd1b76148f2a

  • NADAC price for package 83980000201

    GET /v1/drugs/nadac/83980000201

  • NADAC price for package 83980000210

    GET /v1/drugs/nadac/83980000210

Use it

Look up 83980-002 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/83980-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 83980-002. 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.