Package 68180-376-09

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 68180-376-09
Digits Only 6818037609
Product NDC 68180-376
Product ID 68180-376_38431fb6-7157-4be5-929a-0c65b7a29c55
Description

90 TABLET in 1 BOTTLE (68180-376-09)

Marketing

Marketing Status
Marketed Since 2017-11-01
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": "38431fb6-7157-4be5-929a-0c65b7a29c55", "openfda": {"upc": ["0368180212065", "0368180376033", "0368180210061", "0368180378037", "0368180308027", "0368180376095", "0368180211068", "0368180309024", "0368180377030"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["e5886220-43b7-46e1-9034-5242ba245bd1"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (68180-376-03)", "package_ndc": "68180-376-03", "marketing_start_date": "20171101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68180-376-09)", "package_ndc": "68180-376-09", "marketing_start_date": "20171101"}], "brand_name": "Losartan Potassium", "product_id": "68180-376_38431fb6-7157-4be5-929a-0c65b7a29c55", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68180-376", "generic_name": "Losartan Potassium", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA078232", "marketing_category": "ANDA", "marketing_start_date": "20171101", "listing_expiration_date": "20271231"}