Package 68071-2690-3

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 68071-2690-3
Digits Only 6807126903
Product NDC 68071-2690
Product ID 68071-2690_2a33f0af-89aa-eeb3-e063-6394a90af0ca
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-2690-3)

Marketing

Marketing Status
Marketed Since 2022-05-06
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": "2a33f0af-89aa-eeb3-e063-6394a90af0ca", "openfda": {"upc": ["0368071269031"], "unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["de5c0c87-e90b-fc14-e053-2a95a90af0c5"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-2690-3)", "package_ndc": "68071-2690-3", "marketing_start_date": "20220506"}], "brand_name": "Losartan Potassium", "product_id": "68071-2690_2a33f0af-89aa-eeb3-e063-6394a90af0ca", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68071-2690", "generic_name": "Losartan potassium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA091497", "marketing_category": "ANDA", "marketing_start_date": "20140730", "listing_expiration_date": "20261231"}