Package 69584-023-50

Brand: amlodipine besylate 10 mg

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 69584-023-50
Digits Only 6958402350
Product NDC 69584-023
Product ID 69584-023_37bc3d9c-697e-4dbd-96e4-daba4873840c
Description

500 TABLET in 1 BOTTLE (69584-023-50)

Marketing

Marketing Status
Marketed Since 2021-10-01
Brand amlodipine besylate 10 mg
Generic amlodipine besylate
Sample Package No

Linked Drug Pages (1)

AMLODIPINE BESYLATE 2.5 mg, AMLODIPINE BESYLATE 5 mg, AMLODIPINE BESYLATE 10 mg ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "37bc3d9c-697e-4dbd-96e4-daba4873840c", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["197361", "308135", "308136"], "spl_set_id": ["6f20efca-943b-4bc2-a157-0931bd4d4585"], "manufacturer_name": ["Oxford Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (69584-023-09)", "package_ndc": "69584-023-09", "marketing_start_date": "20211001"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69584-023-50)", "package_ndc": "69584-023-50", "marketing_start_date": "20211001"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69584-023-90)", "package_ndc": "69584-023-90", "marketing_start_date": "20211001"}, {"sample": false, "description": "3000 TABLET in 1 BOTTLE (69584-023-93)", "package_ndc": "69584-023-93", "marketing_start_date": "20211001"}, {"sample": false, "description": "5000 TABLET in 1 BOTTLE (69584-023-95)", "package_ndc": "69584-023-95", "marketing_start_date": "20211001"}], "brand_name": "AMLODIPINE BESYLATE 10 mg", "product_id": "69584-023_37bc3d9c-697e-4dbd-96e4-daba4873840c", "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": "69584-023", "generic_name": "AMLODIPINE BESYLATE", "labeler_name": "Oxford Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMLODIPINE BESYLATE", "brand_name_suffix": "10 mg", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}], "application_number": "ANDA078414", "marketing_category": "ANDA", "marketing_start_date": "20211001", "listing_expiration_date": "20261231"}