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ETHACRYNATE SODIUM

NDC 69315-701, ETHACRYNATE SODIUM, injection, powder, lyophilized, for solution, from Leading Pharma, LLC.

Product NDC
69315-701
Status
Listed
Labeler
Leading Pharma, LLC
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208663
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69315-701 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ETHACRYNATE SODIUM50 mg/50mL

Pharmacologic classes

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

Package NDCNDC-11Package
69315-701-50693150701501 VIAL, SINGLE-DOSE in 1 CARTON (69315-701-50) / 50 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e24e7440-a958-6fd0-6bfe-1bd29e638657

Use it

Look up 69315-701 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69315-701 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69315-701. 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.