Package 0480-0083-05
Brand: amlodipine besylate
Generic: amlodipine besylatePackage Facts
Identity
Package NDC
0480-0083-05
Digits Only
0480008305
Product NDC
0480-0083
Description
500 TABLET in 1 BOTTLE (0480-0083-05)
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": "2e80607e-f2c3-4966-b360-4b39d3d1dfd1", "openfda": {"upc": ["0304807167981"], "unii": ["864V2Q084H"], "rxcui": ["197361", "308135", "308136"], "spl_set_id": ["47edc328-2444-4ca1-a5c1-7c83141e105c"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (0480-0083-05)", "package_ndc": "0480-0083-05", "marketing_start_date": "20230511"}], "brand_name": "Amlodipine Besylate", "product_id": "0480-0083_2e80607e-f2c3-4966-b360-4b39d3d1dfd1", "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": "0480-0083", "generic_name": "Amlodipine Besylate", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "2.5 mg/1"}], "application_number": "ANDA076846", "marketing_category": "ANDA", "marketing_start_date": "20221001", "listing_expiration_date": "20261231"}