Package 82009-073-90

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 82009-073-90
Digits Only 8200907390
Product NDC 82009-073
Description

90 TABLET, FILM COATED in 1 BOTTLE (82009-073-90)

Marketing

Marketing Status
Marketed Since 2023-08-01
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": "477067c5-6637-417d-8b4d-5efb555272eb", "openfda": {"upc": ["0382009073903"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["98f930d5-f7c2-4870-92b4-0ad37ce45797"], "manufacturer_name": ["QUALLENT PHARMACEUTICALS HEALTH LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82009-073-90)", "package_ndc": "82009-073-90", "marketing_start_date": "20230801"}], "brand_name": "Olmesartan Medoxomil", "product_id": "82009-073_477067c5-6637-417d-8b4d-5efb555272eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "82009-073", "generic_name": "Olmesartan Medoxomil", "labeler_name": "QUALLENT PHARMACEUTICALS HEALTH LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "5 mg/1"}], "application_number": "ANDA204798", "marketing_category": "ANDA", "marketing_start_date": "20230801", "listing_expiration_date": "20261231"}