Package 60760-858-90

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 60760-858-90
Digits Only 6076085890
Product NDC 60760-858
Description

90 TABLET in 1 BOTTLE, PLASTIC (60760-858-90)

Marketing

Marketing Status
Marketed Since 2023-06-15
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": "febeaf96-c9fb-c5a8-e053-6294a90ac179", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["febeaf8c-0f4b-cc40-e053-6394a90a873e"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-858-90)", "package_ndc": "60760-858-90", "marketing_start_date": "20230615"}], "brand_name": "Furosemide", "product_id": "60760-858_febeaf96-c9fb-c5a8-e053-6294a90ac179", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "60760-858", "generic_name": "Furosemide", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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": "20230615", "listing_expiration_date": "20261231"}