Package 42571-203-30

{"route": ["ORAL"], "spl_id": "3619c2a8-fac7-3b89-e063-6294a90a7209", "openfda": {"upc": ["0342571201302", "0342571203306", "0342571202309"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["de799a31-50ae-4b9e-a159-3d399b523dca"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (42571-203-05)", "package_ndc": "42571-203-05", "marketing_start_date": "20200203"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (42571-203-10)", "package_ndc": "42571-203-10", "marketing_start_date": "20200203"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (42571-203-11)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-203-32)", "package_ndc": "42571-203-11", "marketing_start_date": "20200203"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42571-203-30)", "package_ndc": "42571-203-30", "marketing_start_date": "20200203"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (42571-203-90)", "package_ndc": "42571-203-90", "marketing_start_date": "20200203"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "42571-203_3619c2a8-fac7-3b89-e063-6294a90a7209", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "42571-203", "generic_name": "olmesartan medoxomil", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA206372", "marketing_category": "ANDA", "marketing_start_date": "20200203", "listing_expiration_date": "20261231"}