Package 67046-1470-3

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 67046-1470-3
Digits Only 6704614703
Product NDC 67046-1470
Product ID 67046-1470_2d55243e-d784-601f-e063-6394a90ab498
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1470-3)

Marketing

Marketing Status
Marketed Since 2025-02-04
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": "2d55243e-d784-601f-e063-6394a90ab498", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["2d5524d5-c76b-44af-e063-6294a90a2ef1"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1470-3)", "package_ndc": "67046-1470-3", "marketing_start_date": "20250204"}], "brand_name": "Losartan potassium", "product_id": "67046-1470_2d55243e-d784-601f-e063-6394a90ab498", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "67046-1470", "generic_name": "Losartan potassium", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA217396", "marketing_category": "ANDA", "marketing_start_date": "20250204", "listing_expiration_date": "20261231"}