Package 68382-135-01

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 68382-135-01
Digits Only 6838213501
Product NDC 68382-135
Description

100 TABLET, FILM COATED in 1 BOTTLE (68382-135-01)

Marketing

Marketing Status
Marketed Since 2010-10-04
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a4867c6-b625-44bf-ad89-79eaf2e490df", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["3233c707-70b6-4c29-8210-913eeb2a38ed"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68382-135-01)", "package_ndc": "68382-135-01", "marketing_start_date": "20101004"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68382-135-06)", "package_ndc": "68382-135-06", "marketing_start_date": "20101004"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68382-135-10)", "package_ndc": "68382-135-10", "marketing_start_date": "20101004"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68382-135-16)", "package_ndc": "68382-135-16", "marketing_start_date": "20101004"}, {"sample": false, "description": "10000 TABLET, FILM COATED in 1 BOTTLE (68382-135-24)", "package_ndc": "68382-135-24", "marketing_start_date": "20101004"}], "brand_name": "Losartan Potassium", "product_id": "68382-135_0a4867c6-b625-44bf-ad89-79eaf2e490df", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68382-135", "generic_name": "Losartan Potassium", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA078243", "marketing_category": "ANDA", "marketing_start_date": "20101004", "listing_expiration_date": "20271231"}