Package 72189-082-30

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 72189-082-30
Digits Only 7218908230
Product NDC 72189-082
Product ID 72189-082_2be871d4-0d2d-9f90-e063-6294a90ad6d2
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-082-30)

Marketing

Marketing Status
Marketed Since 2020-06-16
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": "2be871d4-0d2d-9f90-e063-6294a90ad6d2", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["a58c56b2-e05c-6697-e053-2a95a90ad466"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-082-30)", "package_ndc": "72189-082-30", "marketing_start_date": "20200616"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-082-90)", "package_ndc": "72189-082-90", "marketing_start_date": "20200616"}], "brand_name": "LOSARTAN POTASSIUM", "product_id": "72189-082_2be871d4-0d2d-9f90-e063-6294a90ad6d2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-082", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "DIRECT RX", "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": "20200616", "listing_expiration_date": "20261231"}