Package 62332-215-30

Brand: amlodipine besylate and olmesartran medoxomil

Generic: amlodipine besylate and olmesartran medoxomil
NDC Package

Package Facts

Identity

Package NDC 62332-215-30
Digits Only 6233221530
Product NDC 62332-215
Description

30 TABLET, FILM COATED in 1 BOTTLE (62332-215-30)

Marketing

Marketing Status
Marketed Since 2017-07-18
Brand amlodipine besylate and olmesartran medoxomil
Generic amlodipine besylate and olmesartran medoxomil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fe578906-d9fc-4f00-9de4-8e02292ad1c0", "openfda": {"upc": ["0362332213306", "0362332215300", "0362332212309", "0362332214303"], "unii": ["864V2Q084H", "6M97XTV3HD"], "rxcui": ["730861", "730866", "730869", "730872"], "spl_set_id": ["1eb78d80-701d-4766-98c3-feee6790de1a"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-215-30)", "package_ndc": "62332-215-30", "marketing_start_date": "20170718"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62332-215-90)", "package_ndc": "62332-215-90", "marketing_start_date": "20170718"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-215-91)", "package_ndc": "62332-215-91", "marketing_start_date": "20170718"}], "brand_name": "Amlodipine besylate and Olmesartran medoxomil", "product_id": "62332-215_fe578906-d9fc-4f00-9de4-8e02292ad1c0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "62332-215", "generic_name": "Amlodipine besylate and Olmesartran medoxomil", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine besylate and Olmesartran medoxomil", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA207073", "marketing_category": "ANDA", "marketing_start_date": "20170718", "listing_expiration_date": "20261231"}