Package 82868-031-90
Brand: amlodipine besylate
Generic: amlodipine besylatePackage Facts
Identity
Package NDC
82868-031-90
Digits Only
8286803190
Product NDC
82868-031
Description
90 TABLET in 1 BOTTLE, PLASTIC (82868-031-90)
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": "46dcab92-b42e-b3f1-e063-6394a90a17c3", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["0de6a6d0-a114-e114-e063-6394a90a34dd"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (82868-031-90)", "package_ndc": "82868-031-90", "marketing_start_date": "20231212"}], "brand_name": "Amlodipine Besylate", "product_id": "82868-031_46dcab92-b42e-b3f1-e063-6394a90a17c3", "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": "82868-031", "generic_name": "Amlodipine Besylate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}], "application_number": "ANDA203245", "marketing_category": "ANDA", "marketing_start_date": "20231212", "listing_expiration_date": "20261231"}