Package 72189-303-90

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 72189-303-90
Digits Only 7218930390
Product NDC 72189-303
Product ID 72189-303_2c295943-f8ca-fd38-e063-6394a90ad5cf
Description

90 TABLET, FILM COATED in 1 BOTTLE (72189-303-90)

Marketing

Marketing Status
Marketed Since 2021-12-17
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": "2c295943-f8ca-fd38-e063-6394a90ad5cf", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["d358499d-5ebb-75b2-e053-2a95a90a4223"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-303-90)", "package_ndc": "72189-303-90", "marketing_start_date": "20211217"}], "brand_name": "Losartan Potassium", "product_id": "72189-303_2c295943-f8ca-fd38-e063-6394a90ad5cf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-303", "generic_name": "Losartan Potassium", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20211217", "listing_expiration_date": "20261231"}