Package 71610-439-60

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 71610-439-60
Digits Only 7161043960
Product NDC 71610-439
Description

90 TABLET, FILM COATED in 1 BOTTLE (71610-439-60)

Marketing

Marketing Status
Marketed Since 2022-10-17
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": "ac858720-a7ec-4205-a13b-596c948cde60", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485", "979492"], "spl_set_id": ["8015c22c-d944-4a49-8721-70d0c1b98526"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71610-439-15)", "package_ndc": "71610-439-15", "marketing_start_date": "20210427"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-439-30)", "package_ndc": "71610-439-30", "marketing_start_date": "20200624"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71610-439-45)", "package_ndc": "71610-439-45", "marketing_start_date": "20210315"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-439-60)", "package_ndc": "71610-439-60", "marketing_start_date": "20221017"}], "brand_name": "LOSARTAN POTASSIUM", "product_id": "71610-439_ac858720-a7ec-4205-a13b-596c948cde60", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71610-439", "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": "25 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20200313", "listing_expiration_date": "20261231"}