Package 68071-4943-9

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 68071-4943-9
Digits Only 6807149439
Product NDC 68071-4943
Product ID 68071-4943_1b2e1fc4-f5f9-9895-e063-6394a90ad067
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-4943-9)

Marketing

Marketing Status
Marketed Since 2019-06-25
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": "1b2e1fc4-f5f9-9895-e063-6394a90ad067", "openfda": {"upc": ["0368071494396"], "unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["8c2b3412-254b-8fa9-e053-2a95a90a7dc6"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-4943-9)", "package_ndc": "68071-4943-9", "marketing_start_date": "20190625"}], "brand_name": "Losartan Potassium", "product_id": "68071-4943_1b2e1fc4-f5f9-9895-e063-6394a90ad067", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68071-4943", "generic_name": "Losartan Potassium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}