Package 82009-026-10

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 82009-026-10
Digits Only 8200902610
Product NDC 82009-026
Description

1000 TABLET in 1 BOTTLE (82009-026-10)

Marketing

Marketing Status
Marketed Since 2023-12-15
Brand amlodipine besylate
Generic amlodipine besylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "72ad7e01-b3db-46b3-af3f-746e5ec70cd0", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["197361", "308135", "308136"], "spl_set_id": ["c262dedb-1d13-4447-9355-f11e1dbbfb4d"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (82009-026-10)", "package_ndc": "82009-026-10", "marketing_start_date": "20231215"}], "brand_name": "AMLODIPINE BESYLATE", "product_id": "82009-026_72ad7e01-b3db-46b3-af3f-746e5ec70cd0", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "82009-026", "generic_name": "AMLODIPINE BESYLATE", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMLODIPINE BESYLATE", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "2.5 mg/1"}], "application_number": "ANDA077073", "marketing_category": "ANDA", "marketing_start_date": "20221201", "listing_expiration_date": "20261231"}