Package 50090-6714-0

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 50090-6714-0
Digits Only 5009067140
Product NDC 50090-6714
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6714-0)

Marketing

Marketing Status
Marketed Since 2023-10-04
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39775c40-a0bd-4981-be4e-0ea1cfa7c321", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["cff0c9eb-fafd-48e7-a053-036b676bf57d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6714-0)", "package_ndc": "50090-6714-0", "marketing_start_date": "20231004"}], "brand_name": "Losartan Potassium", "product_id": "50090-6714_39775c40-a0bd-4981-be4e-0ea1cfa7c321", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-6714", "generic_name": "Losartan Potassium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}