Package 70518-4289-0

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 70518-4289-0
Digits Only 7051842890
Product NDC 70518-4289
Product ID 70518-4289_401bdca5-0e36-b15d-e063-6294a90a5732
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4289-0)

Marketing

Marketing Status
Marketed Since 2025-02-14
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Losartan potassium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "401bdca5-0e36-b15d-e063-6294a90a5732", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["a397502e-abe7-49cf-97c7-d53a616947eb"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4289-0)", "package_ndc": "70518-4289-0", "marketing_start_date": "20250214"}], "brand_name": "Losartan potassium", "product_id": "70518-4289_401bdca5-0e36-b15d-e063-6294a90a5732", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-4289", "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": "ANDA202230", "marketing_category": "ANDA", "marketing_start_date": "20250214", "listing_expiration_date": "20261231"}