Package 67296-1876-9

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 67296-1876-9
Digits Only 6729618769
Product NDC 67296-1876
Description

30 TABLET in 1 BOTTLE (67296-1876-9)

Marketing

Marketing Status
Marketed Since 2020-06-22
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": "2c62f690-8df4-d28e-e063-6394a90a45a2", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["197361"], "spl_set_id": ["fc61eee9-ee15-9078-e053-6394a90a22f4"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-1876-9)", "package_ndc": "67296-1876-9", "marketing_start_date": "20200622"}], "brand_name": "Amlodipine Besylate", "product_id": "67296-1876_2c62f690-8df4-d28e-e063-6394a90a45a2", "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": "67296-1876", "generic_name": "Amlodipine Besylate", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}], "application_number": "ANDA203245", "marketing_category": "ANDA", "marketing_start_date": "20190522", "listing_expiration_date": "20261231"}