Package 50090-7795-0

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 50090-7795-0
Digits Only 5009077950
Product NDC 50090-7795
Product ID 50090-7795_ff0c06e7-4597-43f9-8bfe-298f7607ba28
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7795-0)

Marketing

Marketing Status
Marketed Since 2025-11-25
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ff0c06e7-4597-43f9-8bfe-298f7607ba28", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["d1000341-9f81-403f-a8e4-55e1eead432a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7795-0)", "package_ndc": "50090-7795-0", "marketing_start_date": "20251125"}], "brand_name": "Losartan Potassium", "product_id": "50090-7795_ff0c06e7-4597-43f9-8bfe-298f7607ba28", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-7795", "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": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20261231"}