Package 68071-2203-9

Brand: losartan potassium 100 mg

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 68071-2203-9
Digits Only 6807122039
Product NDC 68071-2203
Product ID 68071-2203_1d75df72-5359-f395-e063-6394a90a2fb3
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-2203-9)

Marketing

Marketing Status
Marketed Since 2020-06-30
Brand losartan potassium 100 mg
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

LOSARTAN POTASSIUM 100 mg ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d75df72-5359-f395-e063-6394a90a2fb3", "openfda": {"upc": ["0368071220391"], "unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["a955160f-3c2d-3366-e053-2a95a90a65ea"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-2203-9)", "package_ndc": "68071-2203-9", "marketing_start_date": "20200630"}], "brand_name": "LOSARTAN POTASSIUM 100 mg", "product_id": "68071-2203_1d75df72-5359-f395-e063-6394a90a2fb3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68071-2203", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "brand_name_suffix": "100 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA090382", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20261231"}