Package 71205-281-30

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 71205-281-30
Digits Only 7120528130
Product NDC 71205-281
Product ID 71205-281_3acdf264-82c4-4635-bd40-e80e6d8fb3f8
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-281-30)

Marketing

Marketing Status
Marketed Since 2019-06-01
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": "3acdf264-82c4-4635-bd40-e80e6d8fb3f8", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["44050993-c20e-45d4-baeb-f77d91296168"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-281-30)", "package_ndc": "71205-281-30", "marketing_start_date": "20190601"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-281-60)", "package_ndc": "71205-281-60", "marketing_start_date": "20190601"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-281-90)", "package_ndc": "71205-281-90", "marketing_start_date": "20190601"}], "brand_name": "Losartan Potassium", "product_id": "71205-281_3acdf264-82c4-4635-bd40-e80e6d8fb3f8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71205-281", "generic_name": "Losartan Potassium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}