Package 68084-346-01

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 68084-346-01
Digits Only 6808434601
Product NDC 68084-346
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-346-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-346-11)

Marketing

Marketing Status
Marketed Since 2010-10-12
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": "23aa9d46-bb06-0f79-e063-6394a90a21a0", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["e7f6b25b-ec4c-4c3a-a541-617d2d9ab393"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-346-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-346-11)", "package_ndc": "68084-346-01", "marketing_start_date": "20101012"}], "brand_name": "Losartan Potassium", "product_id": "68084-346_23aa9d46-bb06-0f79-e063-6394a90a21a0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68084-346", "generic_name": "Losartan Potassium", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA078243", "marketing_category": "ANDA", "marketing_start_date": "20101012", "listing_expiration_date": "20261231"}