Package 71610-465-60

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 71610-465-60
Digits Only 7161046560
Product NDC 71610-465
Description

90 TABLET, FILM COATED in 1 BOTTLE (71610-465-60)

Marketing

Marketing Status
Marketed Since 2020-09-15
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": "03a7d931-b0de-41e6-99e0-0d4ff6cb78b8", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["2f738295-53d6-4d4f-8864-9faf893dbdf2"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-465-30)", "package_ndc": "71610-465-30", "marketing_start_date": "20200915"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-465-60)", "package_ndc": "71610-465-60", "marketing_start_date": "20200915"}], "brand_name": "LOSARTAN POTASSIUM", "product_id": "71610-465_03a7d931-b0de-41e6-99e0-0d4ff6cb78b8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71610-465", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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": "20200313", "listing_expiration_date": "20261231"}