Package 50090-6853-0
Brand: amlodipine besylate
Generic: amlodipine besylatePackage Facts
Identity
Package NDC
50090-6853-0
Digits Only
5009068530
Product NDC
50090-6853
Description
90 TABLET in 1 BOTTLE (50090-6853-0)
Marketing
Marketing Status
Brand
amlodipine besylate
Generic
amlodipine besylate
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a133e010-5957-430e-b449-aae85224caab", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["308136"], "spl_set_id": ["00a037f6-b17f-4d21-9a9a-0e682f68d483"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6853-0)", "package_ndc": "50090-6853-0", "marketing_start_date": "20231129"}], "brand_name": "Amlodipine Besylate", "product_id": "50090-6853_a133e010-5957-430e-b449-aae85224caab", "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": "50090-6853", "generic_name": "Amlodipine besylate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "2.5 mg/1"}], "application_number": "ANDA078925", "marketing_category": "ANDA", "marketing_start_date": "20101020", "listing_expiration_date": "20261231"}