Package 69315-701-50

Brand: ethacrynate sodium

Generic: ethacrynate sodium
NDC Package

Package Facts

Identity

Package NDC 69315-701-50
Digits Only 6931570150
Product NDC 69315-701
Product ID 69315-701_f2c45a04-b3df-48cd-93e2-edb917a029cf
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (69315-701-50) / 50 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2026-01-09
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": "f2c45a04-b3df-48cd-93e2-edb917a029cf", "openfda": {"upc": ["0369315701508"], "unii": ["K41MYV7MPM"], "rxcui": ["617325"], "spl_set_id": ["e24e7440-a958-6fd0-6bfe-1bd29e638657"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (69315-701-50)  / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "69315-701-50", "marketing_start_date": "20260109"}], "brand_name": "ETHACRYNATE SODIUM", "product_id": "69315-701_f2c45a04-b3df-48cd-93e2-edb917a029cf", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "69315-701", "generic_name": "ETHACRYNATE SODIUM", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ETHACRYNATE SODIUM", "active_ingredients": [{"name": "ETHACRYNATE SODIUM", "strength": "50 mg/50mL"}], "application_number": "ANDA208663", "marketing_category": "ANDA", "marketing_start_date": "20260109", "listing_expiration_date": "20271231"}