Package 50090-6937-0

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 50090-6937-0
Digits Only 5009069370
Product NDC 50090-6937
Description

90 TABLET in 1 BOTTLE (50090-6937-0)

Marketing

Marketing Status
Marketed Since 2023-12-15
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": "f1e4d5a1-fc65-47ce-b6bd-47b1c793dccf", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["60cf5e60-9a7a-42c2-95b5-016f7a68ffc4"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6937-0)", "package_ndc": "50090-6937-0", "marketing_start_date": "20231215"}], "brand_name": "Furosemide", "product_id": "50090-6937_f1e4d5a1-fc65-47ce-b6bd-47b1c793dccf", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-6937", "generic_name": "Furosemide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20060201", "listing_expiration_date": "20261231"}