Package 70518-4316-0

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 70518-4316-0
Digits Only 7051843160
Product NDC 70518-4316
Product ID 70518-4316_402e3048-82b6-8323-e063-6294a90ace2b
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4316-0)

Marketing

Marketing Status
Marketed Since 2025-03-20
Brand olmesartan medoxomil
Generic olmesartan medoxomil
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "402e3048-82b6-8323-e063-6294a90ace2b", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401"], "spl_set_id": ["fe6e39da-fb6e-46da-9c03-c765020a7c87"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4316-0)", "package_ndc": "70518-4316-0", "marketing_start_date": "20250320"}], "brand_name": "olmesartan medoxomil", "product_id": "70518-4316_402e3048-82b6-8323-e063-6294a90ace2b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-4316", "generic_name": "olmesartan medoxomil", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA208130", "marketing_category": "ANDA", "marketing_start_date": "20250320", "listing_expiration_date": "20261231"}