Package 31722-701-30

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 31722-701-30
Digits Only 3172270130
Product NDC 31722-701
Product ID 31722-701_40b34aeb-20b5-4200-e063-6394a90a96e9
Description

30 TABLET, FILM COATED in 1 BOTTLE (31722-701-30)

Marketing

Marketing Status
Marketed Since 2015-08-19
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": "40b34aeb-20b5-4200-e063-6394a90a96e9", "openfda": {"upc": ["0331722702300", "0331722700900", "0331722701303"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["cafd54e8-42a8-474c-8ea8-49ec74c2b0d3"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-701-05)", "package_ndc": "31722-701-05", "marketing_start_date": "20150819"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (31722-701-10)", "package_ndc": "31722-701-10", "marketing_start_date": "20150819"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-701-30)", "package_ndc": "31722-701-30", "marketing_start_date": "20150819"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (31722-701-60)", "package_ndc": "31722-701-60", "marketing_start_date": "20150819"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-701-90)", "package_ndc": "31722-701-90", "marketing_start_date": "20150819"}], "brand_name": "Losartan Potassium", "product_id": "31722-701_40b34aeb-20b5-4200-e063-6394a90a96e9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "31722-701", "generic_name": "Losartan Potassium", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20261231"}