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Furosemide

NDC 68788-6784, Furosemide, tablet, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-6784
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/68788-6784 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68788-6784-168788678401100 TABLET in 1 BOTTLE (68788-6784-1)
68788-6784-36878867840330 TABLET in 1 BOTTLE (68788-6784-3)
68788-6784-66878867840660 TABLET in 1 BOTTLE (68788-6784-6)
68788-6784-96878867840990 TABLET in 1 BOTTLE (68788-6784-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a23fc1e0-2d16-43a8-a34e-f6505dcd6316

Use it

Look up 68788-6784 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-6784 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-6784. 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.