Package 72189-520-30
Brand: amlodipine besylate
Generic: amlodipine besylatePackage Facts
Identity
Package NDC
72189-520-30
Digits Only
7218952030
Product NDC
72189-520
Description
30 TABLET in 1 BOTTLE (72189-520-30)
Marketing
Marketing Status
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": "1ac60230-47d7-d920-e063-6294a90a4929", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["197361"], "spl_set_id": ["094498f2-11d9-2a05-e063-6294a90ab2e1"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-520-30)", "package_ndc": "72189-520-30", "marketing_start_date": "20231103"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-520-90)", "package_ndc": "72189-520-90", "marketing_start_date": "20231103"}], "brand_name": "Amlodipine Besylate", "product_id": "72189-520_1ac60230-47d7-d920-e063-6294a90a4929", "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": "72189-520", "generic_name": "Amlodipine Besylate", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}], "application_number": "ANDA203245", "marketing_category": "ANDA", "marketing_start_date": "20231103", "listing_expiration_date": "20261231"}