Package 31722-853-30

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 31722-853-30
Digits Only 3172285330
Product NDC 31722-853
Product ID 31722-853_35cb69e0-7e6c-d4ee-e063-6294a90ae48c
Description

30 TABLET, FILM COATED in 1 BOTTLE (31722-853-30)

Marketing

Marketing Status
Marketed Since 2025-05-23
Brand olmesartan medoxomil
Generic olmesartan medoxomil
Sample Package No

Linked Drug Pages (1)

OLMESARTAN MEDOXOMIL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35cb69e0-7e6c-d4ee-e063-6294a90ae48c", "openfda": {"upc": ["0331722854306", "0331722852302", "0331722853309"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["53b8d406-a4f3-46ee-9aec-d70f7d806876"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-853-30)", "package_ndc": "31722-853-30", "marketing_start_date": "20250523"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-853-90)", "package_ndc": "31722-853-90", "marketing_start_date": "20250523"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "31722-853_35cb69e0-7e6c-d4ee-e063-6294a90ae48c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "31722-853", "generic_name": "OLMESARTAN MEDOXOMIL", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA205499", "marketing_category": "ANDA", "marketing_start_date": "20250523", "listing_expiration_date": "20261231"}