Package 72189-138-30
Brand: olmesartan medoxomil
Generic: olmesartan medoxomilPackage Facts
Identity
Package NDC
72189-138-30
Digits Only
7218913830
Product NDC
72189-138
Description
30 TABLET, FILM COATED in 1 BOTTLE (72189-138-30)
Marketing
Marketing Status
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": "2becff06-7cc1-1200-e063-6294a90ad1ec", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401", "349405"], "spl_set_id": ["b57e47a5-43e0-d1c5-e053-2a95a90a2b07"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-138-30)", "package_ndc": "72189-138-30", "marketing_start_date": "20201202"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-138-90)", "package_ndc": "72189-138-90", "marketing_start_date": "20201202"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "72189-138_2becff06-7cc1-1200-e063-6294a90ad1ec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-138", "generic_name": "OLMESARTAN MEDOXOMIL", "labeler_name": "direct rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA207662", "marketing_category": "ANDA", "marketing_start_date": "20201202", "listing_expiration_date": "20261231"}