Package 70518-1343-0

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 70518-1343-0
Digits Only 7051813430
Product NDC 70518-1343
Product ID 70518-1343_48e8efeb-67cd-1cd3-e063-6294a90a2dc1
Description

90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1343-0)

Marketing

Marketing Status
Marketed Since 2018-08-06
Brand olmesartan medoxomil
Generic olmesartan medoxomil
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": "48e8efeb-67cd-1cd3-e063-6294a90a2dc1", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401"], "spl_set_id": ["92969ed0-8dcd-4c6d-b0c4-e8469c2f65a9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1343-0)", "package_ndc": "70518-1343-0", "marketing_start_date": "20180806"}], "brand_name": "Olmesartan Medoxomil", "product_id": "70518-1343_48e8efeb-67cd-1cd3-e063-6294a90a2dc1", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-1343", "generic_name": "Olmesartan Medoxomil", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA206763", "marketing_category": "ANDA", "marketing_start_date": "20180806", "listing_expiration_date": "20271231"}