Package 65862-202-30

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 65862-202-30
Digits Only 6586220230
Product NDC 65862-202
Product ID 65862-202_1942e030-0f36-4f65-9f60-4898439afc61
Description

30 TABLET, FILM COATED in 1 BOTTLE (65862-202-30)

Marketing

Marketing Status
Marketed Since 2010-10-06
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": "1942e030-0f36-4f65-9f60-4898439afc61", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["31366b4b-dfd6-4fda-babe-2cb3d2c14a2b"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-202-30)", "package_ndc": "65862-202-30", "marketing_start_date": "20101006"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-202-90)", "package_ndc": "65862-202-90", "marketing_start_date": "20101006"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-202-99)", "package_ndc": "65862-202-99", "marketing_start_date": "20101006"}], "brand_name": "Losartan Potassium", "product_id": "65862-202_1942e030-0f36-4f65-9f60-4898439afc61", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "65862-202", "generic_name": "Losartan Potassium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}