Package 72789-282-30

Brand: losartan potassium 25 mg

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 72789-282-30
Digits Only 7278928230
Product NDC 72789-282
Product ID 72789-282_4bada0ba-e109-3fd8-e063-6394a90a058f
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-282-30)

Marketing

Marketing Status
Marketed Since 2022-10-24
Brand losartan potassium 25 mg
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

LOSARTAN POTASSIUM 25 mg ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4bada0ba-e109-3fd8-e063-6394a90a058f", "openfda": {"upc": ["0372789282305"], "unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["4d60e755-40a6-4187-b09e-e55c735945aa"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-282-30)", "package_ndc": "72789-282-30", "marketing_start_date": "20221024"}], "brand_name": "LOSARTAN POTASSIUM 25 mg", "product_id": "72789-282_4bada0ba-e109-3fd8-e063-6394a90a058f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72789-282", "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"}