Package 68071-3846-3

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 68071-3846-3
Digits Only 6807138463
Product NDC 68071-3846
Product ID 68071-3846_351d4de0-4f1e-9ac7-e063-6394a90a6b21
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-3846-3)

Marketing

Marketing Status
Marketed Since 2025-05-14
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": "351d4de0-4f1e-9ac7-e063-6394a90a6b21", "openfda": {"upc": ["0368071384635"], "unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["351d3c5c-05c6-921a-e063-6394a90abef9"], "manufacturer_name": ["NuCare Pharmaceuticals.Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3846-3)", "package_ndc": "68071-3846-3", "marketing_start_date": "20250514"}], "brand_name": "Losartan Potassium", "product_id": "68071-3846_351d4de0-4f1e-9ac7-e063-6394a90a6b21", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68071-3846", "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": "100 mg/1"}], "application_number": "ANDA091497", "marketing_category": "ANDA", "marketing_start_date": "20220320", "listing_expiration_date": "20261231"}