Package 42708-152-30

Brand: losartan potassium

Generic: losartan potassium
NDC Package Sample

Package Facts

Identity

Package NDC 42708-152-30
Digits Only 4270815230
Product NDC 42708-152
Product ID 42708-152_4682352a-49a0-d793-e063-6394a90a4514
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-152-30)

Marketing

Marketing Status
Marketed Since 2021-07-30
Brand losartan potassium
Generic losartan potassium
Sample Package Yes

Linked Drug Pages (1)

Losartan Potassium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4682352a-49a0-d793-e063-6394a90a4514", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["c80b3a28-ef15-5902-e053-2995a90a06d7"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-152-30)", "package_ndc": "42708-152-30", "marketing_start_date": "20210730"}], "brand_name": "Losartan Potassium", "product_id": "42708-152_4682352a-49a0-d793-e063-6394a90a4514", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "42708-152", "generic_name": "Losartan Potassium", "labeler_name": "QPharma, Inc.", "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"}