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Furosemide

NDC 68788-6948, Furosemide, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-6948
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077293
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-6948 \
  -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
68788-6948-168788694801100 TABLET in 1 BOTTLE (68788-6948-1)
68788-6948-36878869480330 TABLET in 1 BOTTLE (68788-6948-3)
68788-6948-66878869480660 TABLET in 1 BOTTLE (68788-6948-6)
68788-6948-96878869480990 TABLET in 1 BOTTLE (68788-6948-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cad102d7-0197-4cff-bb80-9f0b5bcb599b

Use it

Look up 68788-6948 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-6948 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-6948. 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.