Package 72789-163-90

Brand: losartan potassium 25 mg

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 72789-163-90
Digits Only 7278916390
Product NDC 72789-163
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-163-90)

Marketing

Marketing Status
Marketed Since 2021-02-03
Brand losartan potassium 25 mg
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4af79dfe-6b5c-ba11-e063-6294a90aca69", "openfda": {"upc": ["0372789163901", "0372789164908", "0372789165905"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["372ba4ad-26ca-4675-8475-4b664fbecba9"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-163-90)", "package_ndc": "72789-163-90", "marketing_start_date": "20210203"}], "brand_name": "LOSARTAN POTASSIUM 25 mg", "product_id": "72789-163_4af79dfe-6b5c-ba11-e063-6294a90aca69", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72789-163", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "brand_name_suffix": "25 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA090382", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20271231"}