Package 67046-1510-3

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 67046-1510-3
Digits Only 6704615103
Product NDC 67046-1510
Product ID 67046-1510_2d1ad3cf-2474-bcba-e063-6294a90a6054
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1510-3)

Marketing

Marketing Status
Marketed Since 2025-02-01
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": "2d1ad3cf-2474-bcba-e063-6294a90a6054", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["2d1b1648-8b24-cf4f-e063-6294a90afdd8"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1510-3)", "package_ndc": "67046-1510-3", "marketing_start_date": "20250201"}], "brand_name": "Losartan potassium", "product_id": "67046-1510_2d1ad3cf-2474-bcba-e063-6294a90a6054", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "67046-1510", "generic_name": "Losartan potassium", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA202230", "marketing_category": "ANDA", "marketing_start_date": "20250201", "listing_expiration_date": "20261231"}