Package 42023-157-01

Brand: ethacrynate sodium

Generic: ethacrynate sodium
NDC Package

Package Facts

Identity

Package NDC 42023-157-01
Digits Only 4202315701
Product NDC 42023-157
Product ID 42023-157_923d3573-ccd0-4c71-82e3-6167a23b9161
Description

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

Marketing

Marketing Status
Marketed Since 2015-07-30
Brand ethacrynate sodium
Generic ethacrynate sodium
Sample Package No

Linked Drug Pages (1)

ETHACRYNATE SODIUM ndc-match (0.95)

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"}