Package 68071-5041-9

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 68071-5041-9
Digits Only 6807150419
Product NDC 68071-5041
Product ID 68071-5041_1b410ccc-1bd8-2ee4-e063-6394a90aed60
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-5041-9)

Marketing

Marketing Status
Marketed Since 2019-08-28
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": "1b410ccc-1bd8-2ee4-e063-6394a90aed60", "openfda": {"upc": ["0368071504194"], "unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["9130921b-02f0-82d6-e053-2995a90a9c0a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-5041-9)", "package_ndc": "68071-5041-9", "marketing_start_date": "20190828"}], "brand_name": "Losartan Potassium", "product_id": "68071-5041_1b410ccc-1bd8-2ee4-e063-6394a90aed60", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68071-5041", "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": "25 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}