Package 50090-4914-0

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 50090-4914-0
Digits Only 5009049140
Product NDC 50090-4914
Product ID 50090-4914_2c965949-e86b-43a2-a847-c54ee187280b
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-4914-0)

Marketing

Marketing Status
Marketed Since 2020-02-18
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Losartan Potassium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c965949-e86b-43a2-a847-c54ee187280b", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["f68fd1a2-1cbf-47c8-b8c4-df49cf17540e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-4914-0)", "package_ndc": "50090-4914-0", "marketing_start_date": "20200218"}], "brand_name": "Losartan Potassium", "product_id": "50090-4914_2c965949-e86b-43a2-a847-c54ee187280b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-4914", "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": "100 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20261231"}