Package 68645-599-54

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 68645-599-54
Digits Only 6864559954
Product NDC 68645-599
Product ID 68645-599_47433131-14e4-7dc8-e063-6394a90a0090
Description

30 TABLET, FILM COATED in 1 BOTTLE (68645-599-54)

Marketing

Marketing Status
Marketed Since 2022-08-08
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": "47433131-14e4-7dc8-e063-6394a90a0090", "openfda": {"upc": ["0368645599540"], "unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["e5bddb89-37d3-86d0-e053-2a95a90af4f4"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68645-599-54)", "package_ndc": "68645-599-54", "marketing_start_date": "20220808"}], "brand_name": "Losartan Potassium", "product_id": "68645-599_47433131-14e4-7dc8-e063-6394a90a0090", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68645-599", "generic_name": "Losartan potassium", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "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"}