Package 72789-157-01

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 72789-157-01
Digits Only 7278915701
Product NDC 72789-157
Description

100 TABLET in 1 BOTTLE, PLASTIC (72789-157-01)

Marketing

Marketing Status
Marketed Since 2021-01-12
Brand furosemide
Generic furosemide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3caa7e9c-27aa-08ee-e063-6394a90a08ea", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["48d8f490-e9d1-4c95-ab2f-414d3f4a9df4"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-157-01)", "package_ndc": "72789-157-01", "marketing_start_date": "20210112"}], "brand_name": "Furosemide", "product_id": "72789-157_3caa7e9c-27aa-08ee-e063-6394a90a08ea", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72789-157", "generic_name": "furosemide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}