Package 71610-466-30

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 71610-466-30
Digits Only 7161046630
Product NDC 71610-466
Product ID 71610-466_69881114-634b-432c-8d57-e74e2adb1eb5
Description

30 TABLET, FILM COATED in 1 BOTTLE (71610-466-30)

Marketing

Marketing Status
Marketed Since 2020-09-15
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": "69881114-634b-432c-8d57-e74e2adb1eb5", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["be2432ba-2118-418a-addf-56db9b6c39d2"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-466-30)", "package_ndc": "71610-466-30", "marketing_start_date": "20200915"}], "brand_name": "Losartan Potassium", "product_id": "71610-466_69881114-634b-432c-8d57-e74e2adb1eb5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71610-466", "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": "50 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20261231"}