Package 70756-809-30

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 70756-809-30
Digits Only 7075680930
Product NDC 70756-809
Description

30 TABLET in 1 BOTTLE (70756-809-30)

Marketing

Marketing Status
Marketed Since 2020-05-01
Brand olmesartan medoxomil
Generic olmesartan medoxomil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45810d23-5c40-8cba-e063-6294a90a8e9c", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["a337a621-bf57-4aa4-8224-4356fa2cdbc4"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (70756-809-30)", "package_ndc": "70756-809-30", "marketing_start_date": "20200501"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70756-809-90)", "package_ndc": "70756-809-90", "marketing_start_date": "20200501"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "70756-809_45810d23-5c40-8cba-e063-6294a90a8e9c", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70756-809", "generic_name": "OLMESARTAN MEDOXOMIL", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA207135", "marketing_category": "ANDA", "marketing_start_date": "20200501", "listing_expiration_date": "20261231"}