Package 72789-044-30

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 72789-044-30
Digits Only 7278904430
Product NDC 72789-044
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-044-30)

Marketing

Marketing Status
Marketed Since 2020-01-02
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d5903f1-dad9-a753-e063-6394a90afa9e", "openfda": {"upc": ["0372789044903"], "unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["9b3ddaa2-a835-736a-e053-2995a90aff08"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-044-30)", "package_ndc": "72789-044-30", "marketing_start_date": "20200102"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-044-90)", "package_ndc": "72789-044-90", "marketing_start_date": "20200205"}], "brand_name": "Losartan Potassium", "product_id": "72789-044_2d5903f1-dad9-a753-e063-6394a90afa9e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72789-044", "generic_name": "Losartan Potassium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20261231"}