Package 72162-2257-1

Brand: ethacrynic acid

Generic: ethacrynic acid
NDC Package

Package Facts

Identity

Package NDC 72162-2257-1
Digits Only 7216222571
Product NDC 72162-2257
Description

100 TABLET in 1 BOTTLE (72162-2257-1)

Marketing

Marketing Status
Marketed Since 2019-08-27
Brand ethacrynic acid
Generic ethacrynic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6ee91f7d-ffd8-4045-819a-d0e9764803db", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["M5DP350VZV"], "rxcui": ["1251903"], "spl_set_id": ["fd1b7fb4-fe56-4f2d-860d-bbcea16adfea"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2257-1)", "package_ndc": "72162-2257-1", "marketing_start_date": "20190827"}], "brand_name": "Ethacrynic Acid", "product_id": "72162-2257_6ee91f7d-ffd8-4045-819a-d0e9764803db", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72162-2257", "generic_name": "Ethacrynic Acid", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ethacrynic Acid", "active_ingredients": [{"name": "ETHACRYNIC ACID", "strength": "25 mg/1"}], "application_number": "ANDA211232", "marketing_category": "ANDA", "marketing_start_date": "20190827", "listing_expiration_date": "20261231"}