Package 70518-4464-0
Brand: amlodipine besylate
Generic: amlodipine besylatePackage Facts
Identity
Package NDC
70518-4464-0
Digits Only
7051844640
Product NDC
70518-4464
Description
90 TABLET in 1 BOTTLE, PLASTIC (70518-4464-0)
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": "3de4ec88-b525-d5a5-e063-6294a90ab368", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["3e0fbf93-cc64-4fa5-b586-c2020614c884"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4464-0)", "package_ndc": "70518-4464-0", "marketing_start_date": "20250903"}], "brand_name": "Amlodipine Besylate", "product_id": "70518-4464_3de4ec88-b525-d5a5-e063-6294a90ab368", "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": "70518-4464", "generic_name": "Amlodipine Besylate", "labeler_name": "REMEDYREPACK INC.", "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": "20250903", "listing_expiration_date": "20261231"}