Package 50268-506-15

Brand: losortan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 50268-506-15
Digits Only 5026850615
Product NDC 50268-506
Description

50 BLISTER PACK in 1 BOX (50268-506-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-506-11)

Marketing

Marketing Status
Marketed Since 2020-05-29
Brand losortan 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": "47e73292-3507-3131-e063-6294a90a0de6", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["a6cd0b5f-2bd6-bed9-e053-2995a90a3191"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-506-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-506-11)", "package_ndc": "50268-506-15", "marketing_start_date": "20200529"}], "brand_name": "Losortan Potassium", "product_id": "50268-506_47e73292-3507-3131-e063-6294a90a0de6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50268-506", "generic_name": "Losartan Potassium", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losortan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA078243", "marketing_category": "ANDA", "marketing_start_date": "20200529", "listing_expiration_date": "20271231"}