ethacrynate sodium

Generic: ethacrynate sodium

Labeler: par health usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ethacrynate sodium
Generic Name ethacrynate sodium
Labeler par health usa, llc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

ethacrynate sodium 50 mg/50mL

Manufacturer
Par Health USA, LLC

Identifiers & Regulatory

Product NDC 42023-157
Product ID 42023-157_923d3573-ccd0-4c71-82e3-6167a23b9161
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205473
Listing Expiration 2026-12-31
Marketing Start 2015-07-30

Pharmacologic Class

Classes
increased diuresis at loop of henle [pe] loop diuretic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42023157
Hyphenated Format 42023-157

Supplemental Identifiers

RxCUI
617325
UNII
K41MYV7MPM

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ethacrynate sodium (source: ndc)
Generic Name ethacrynate sodium (source: ndc)
Application Number ANDA205473 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/50mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (42023-157-01) / 50 mL in 1 VIAL
source: ndc

Packages (1)

42023-157-01 1 VIAL in 1 CARTON (42023-157-01) / 50 mL in 1 VIAL

Ingredients (1)

ethacrynate sodium (50 mg/50mL)

Linked Drug Pages (1)

ETHACRYNATE SODIUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "923d3573-ccd0-4c71-82e3-6167a23b9161", "openfda": {"unii": ["K41MYV7MPM"], "rxcui": ["617325"], "spl_set_id": ["3313ed5d-7991-408f-872b-d5a701aa6d83"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (42023-157-01)  / 50 mL in 1 VIAL", "package_ndc": "42023-157-01", "marketing_start_date": "20150730"}], "brand_name": "ETHACRYNATE SODIUM", "product_id": "42023-157_923d3573-ccd0-4c71-82e3-6167a23b9161", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "42023-157", "generic_name": "ethacrynate sodium", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ETHACRYNATE SODIUM", "active_ingredients": [{"name": "ETHACRYNATE SODIUM", "strength": "50 mg/50mL"}], "application_number": "ANDA205473", "marketing_category": "ANDA", "marketing_start_date": "20150730", "listing_expiration_date": "20261231"}