Package 68645-515-54
Brand: amlodipine besylate
Generic: amlodipine besylatePackage Facts
Identity
Package NDC
68645-515-54
Digits Only
6864551554
Product NDC
68645-515
Description
30 TABLET in 1 BOTTLE (68645-515-54)
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": "4c2152ce-6c88-d033-e063-6394a90a90ab", "openfda": {"upc": ["0368645515540", "0368645516547"], "unii": ["864V2Q084H"], "rxcui": ["197361", "308135"], "spl_set_id": ["2cdd0da9-eea6-45e0-b0b7-35413a168a4f"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68645-515-54)", "package_ndc": "68645-515-54", "marketing_start_date": "20160701"}], "brand_name": "Amlodipine Besylate", "product_id": "68645-515_4c2152ce-6c88-d033-e063-6394a90a90ab", "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": "68645-515", "generic_name": "Amlodipine Besylate", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}], "application_number": "ANDA077955", "marketing_category": "ANDA", "marketing_start_date": "20160701", "listing_expiration_date": "20271231"}