Package 68645-580-54

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 68645-580-54
Digits Only 6864558054
Product NDC 68645-580
Description

30 TABLET in 1 BOTTLE (68645-580-54)

Marketing

Marketing Status
Marketed Since 2011-04-25
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": "4c219dee-9f8c-6c56-e063-6294a90accf8", "openfda": {"upc": ["0368645580548"], "unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["215ef2cb-d5b6-43d5-bbd5-195ec57cde2b"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68645-580-54)", "package_ndc": "68645-580-54", "marketing_start_date": "20110425"}], "brand_name": "AMLODIPINE BESYLATE", "product_id": "68645-580_4c219dee-9f8c-6c56-e063-6294a90accf8", "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": "68645-580", "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": "10 mg/1"}], "application_number": "ANDA078552", "marketing_category": "ANDA", "marketing_start_date": "20110425", "listing_expiration_date": "20271231"}