Package 70518-3489-0

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 70518-3489-0
Digits Only 7051834890
Product NDC 70518-3489
Product ID 70518-3489_4af408fb-5d31-b4a7-e063-6294a90a4bb6
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3489-0)

Marketing

Marketing Status
Marketed Since 2022-08-22
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4af408fb-5d31-b4a7-e063-6294a90a4bb6", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["e136356b-e4d2-4e00-a409-35825c5637c9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3489-0)", "package_ndc": "70518-3489-0", "marketing_start_date": "20220822"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3489-2)", "package_ndc": "70518-3489-2", "marketing_start_date": "20260215"}], "brand_name": "Losartan Potassium", "product_id": "70518-3489_4af408fb-5d31-b4a7-e063-6294a90a4bb6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-3489", "generic_name": "Losartan Potassium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA091497", "marketing_category": "ANDA", "marketing_start_date": "20220822", "listing_expiration_date": "20271231"}