Package 0713-0861-30
Brand: benicar
Generic: olmesartan medoxomilPackage Facts
Identity
Package NDC
0713-0861-30
Digits Only
0713086130
Product NDC
0713-0861
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0861-30)
Marketing
Marketing Status
Brand
benicar
Generic
olmesartan medoxomil
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "00494313-514a-b3b5-e063-6294a90a5ad5", "openfda": {"upc": ["0307130861304", "0307130862301", "0307130860307"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405", "352199", "352200", "352201"], "spl_set_id": ["5b6f8a18-8f8a-4521-81c3-3a39c73c6646"], "manufacturer_name": ["Cosette Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0861-30)", "package_ndc": "0713-0861-30", "marketing_start_date": "20220901"}], "brand_name": "Benicar", "product_id": "0713-0861_00494313-514a-b3b5-e063-6294a90a5ad5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "0713-0861", "generic_name": "olmesartan medoxomil", "labeler_name": "Cosette Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benicar", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "NDA021286", "marketing_category": "NDA", "marketing_start_date": "20220901", "listing_expiration_date": "20261231"}