Package 70518-2316-1

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 70518-2316-1
Digits Only 7051823161
Product NDC 70518-2316
Product ID 70518-2316_4a012def-6acb-2b56-e063-6294a90a3184
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2316-1)

Marketing

Marketing Status
Marketed Since 2024-02-14
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": "4a012def-6acb-2b56-e063-6294a90a3184", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["df4f55f0-fb11-4f6f-a7ed-127b50f955fc"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2316-1)", "package_ndc": "70518-2316-1", "marketing_start_date": "20240214"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2316-2)", "package_ndc": "70518-2316-2", "marketing_start_date": "20250320"}], "brand_name": "Losartan Potassium", "product_id": "70518-2316_4a012def-6acb-2b56-e063-6294a90a3184", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-2316", "generic_name": "Losartan Potassium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20190918", "listing_expiration_date": "20271231"}