Package 43063-955-90

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 43063-955-90
Digits Only 4306395590
Product NDC 43063-955
Product ID 43063-955_3fa415e5-6e5f-d2b5-e063-6294a90ad198
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-955-90)

Marketing

Marketing Status
Marketed Since 2019-03-06
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": "3fa415e5-6e5f-d2b5-e063-6294a90ad198", "openfda": {"upc": ["0343063955901"], "unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["5f7612dc-dccf-49e2-b541-3dab9dc1f97a"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-955-90)", "package_ndc": "43063-955-90", "marketing_start_date": "20190306"}], "brand_name": "Losartan Potassium", "product_id": "43063-955_3fa415e5-6e5f-d2b5-e063-6294a90ad198", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "43063-955", "generic_name": "Losartan Potassium", "labeler_name": "PD-Rx 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"}