Package 70518-0959-0

Brand: Losartan Potassium

Generic: Losartan Potassium
NDC Package

Package Facts

Identity

Package NDC 70518-0959-0
Digits Only 7051809590
Product NDC 70518-0959
Product ID 70518-0959_48493ec5-c5f2-0a16-e063-6394a90a3931
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0959-0)

Marketing

Marketing Status
Marketed Since 2018-01-15
Brand Losartan Potassium
Generic Losartan Potassium
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48493ec5-c5f2-0a16-e063-6394a90a3931", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["7f132e13-b657-49d8-9dea-04fc0b8b46d9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0959-0)", "package_ndc": "70518-0959-0", "marketing_start_date": "20180115"}], "brand_name": "Losartan Potassium", "product_id": "70518-0959_48493ec5-c5f2-0a16-e063-6394a90a3931", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-0959", "generic_name": "Losartan Potassium", "labeler_name": "REMEDYREPACK 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": "20180115", "listing_expiration_date": "20271231"}