Package 62135-882-30

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 62135-882-30
Digits Only 6213588230
Product NDC 62135-882
Description

30 TABLET in 1 BOTTLE (62135-882-30)

Marketing

Marketing Status
Marketed Since 2024-04-05
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": "46879df5-2a7d-8b49-e063-6294a90ad4b7", "openfda": {"upc": ["0362135881306", "0362135882303", "0362135880309"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["7835d2b0-8e5d-4d3f-a95f-9252fb65025b"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (62135-882-30)", "package_ndc": "62135-882-30", "marketing_start_date": "20240405"}], "brand_name": "Olmesartan Medoxomil", "product_id": "62135-882_46879df5-2a7d-8b49-e063-6294a90ad4b7", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "62135-882", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA211049", "marketing_category": "ANDA", "marketing_start_date": "20190305", "listing_expiration_date": "20261231"}