Package 70518-0718-1

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 70518-0718-1
Digits Only 7051807181
Product NDC 70518-0718
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0718-1)

Marketing

Marketing Status
Marketed Since 2018-07-20
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48331991-73eb-f827-e063-6394a90a43ca", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["25c93638-7016-47d2-a57c-e4a5245ca41b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0718-0)", "package_ndc": "70518-0718-0", "marketing_start_date": "20170830"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0718-1)", "package_ndc": "70518-0718-1", "marketing_start_date": "20180720"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0718-3)", "package_ndc": "70518-0718-3", "marketing_start_date": "20250320"}], "brand_name": "Losartan Potassium", "product_id": "70518-0718_48331991-73eb-f827-e063-6394a90a43ca", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-0718", "generic_name": "Losartan Potassium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20170830", "listing_expiration_date": "20271231"}