Package 71610-083-30

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 71610-083-30
Digits Only 7161008330
Product NDC 71610-083
Description

30 TABLET, FILM COATED in 1 BOTTLE (71610-083-30)

Marketing

Marketing Status
Marketed Since 2018-06-27
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "231334fb-3368-46d4-80a2-737fda561a05", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["8081b9f8-0b52-46dd-93f2-6bc608b75339"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-083-30)", "package_ndc": "71610-083-30", "marketing_start_date": "20180627"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-083-60)", "package_ndc": "71610-083-60", "marketing_start_date": "20180606"}], "brand_name": "Losartan Potassium", "product_id": "71610-083_231334fb-3368-46d4-80a2-737fda561a05", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71610-083", "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": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}