Package 46708-213-91

Brand: amlodipine besylate and olmesartran medoxomil

Generic: amlodipine besylate and olmesartran medoxomil
NDC Package

Package Facts

Identity

Package NDC 46708-213-91
Digits Only 4670821391
Product NDC 46708-213
Description

1000 TABLET, FILM COATED in 1 BOTTLE (46708-213-91)

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": "cbb564d2-add9-430a-a36b-45147d417138", "openfda": {"upc": ["0346708214302", "0346708212308", "0346708215309", "0346708213305"], "unii": ["864V2Q084H", "6M97XTV3HD"], "rxcui": ["730861", "730866", "730869", "730872"], "spl_set_id": ["cb2df7f7-fee8-42ba-8936-0788c4fcc0cb"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (46708-213-30)", "package_ndc": "46708-213-30", "marketing_start_date": "20170718"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (46708-213-90)", "package_ndc": "46708-213-90", "marketing_start_date": "20170718"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-213-91)", "package_ndc": "46708-213-91", "marketing_start_date": "20170718"}], "brand_name": "Amlodipine besylate and Olmesartran medoxomil", "product_id": "46708-213_cbb564d2-add9-430a-a36b-45147d417138", "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": "46708-213", "generic_name": "Amlodipine besylate and Olmesartran medoxomil", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine besylate and Olmesartran medoxomil", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA207073", "marketing_category": "ANDA", "marketing_start_date": "20170718", "listing_expiration_date": "20261231"}