Package 67296-2139-3

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 67296-2139-3
Digits Only 6729621393
Product NDC 67296-2139
Description

30 TABLET in 1 BOTTLE (67296-2139-3)

Marketing

Marketing Status
Marketed Since 2022-11-05
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": "46acb074-fbbf-c3a2-e063-6394a90a0993", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0364980564014"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["3745be12-ea1d-f450-e063-6294a90a148c"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-2139-3)", "package_ndc": "67296-2139-3", "marketing_start_date": "20221105"}], "brand_name": "Furosemide", "product_id": "67296-2139_46acb074-fbbf-c3a2-e063-6394a90a0993", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "67296-2139", "generic_name": "Furosemide", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA216629", "marketing_category": "ANDA", "marketing_start_date": "20221105", "listing_expiration_date": "20261231"}