Package 43063-954-30

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 43063-954-30
Digits Only 4306395430
Product NDC 43063-954
Product ID 43063-954_3fa404aa-687c-d48c-e063-6394a90a9dc8
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-954-30)

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": "3fa404aa-687c-d48c-e063-6394a90a9dc8", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["f9a92771-5c73-4f17-ac38-29fabfd4a919"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-954-30)", "package_ndc": "43063-954-30", "marketing_start_date": "20190306"}], "brand_name": "Losartan Potassium", "product_id": "43063-954_3fa404aa-687c-d48c-e063-6394a90a9dc8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "43063-954", "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": "100 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}