Package 42291-025-10

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 42291-025-10
Digits Only 4229102510
Product NDC 42291-025
Description

1000 TABLET in 1 BOTTLE (42291-025-10)

Marketing

Marketing Status
Marketed Since 2023-06-22
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": "48481e73-92af-d506-e063-6394a90a6518", "openfda": {"upc": ["0342291025103", "0342291026100"], "unii": ["864V2Q084H"], "rxcui": ["197361", "308135", "308136"], "spl_set_id": ["feb9438a-9cbc-4855-e053-6394a90af15e"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (42291-025-10)", "package_ndc": "42291-025-10", "marketing_start_date": "20230622"}], "brand_name": "Amlodipine Besylate", "product_id": "42291-025_48481e73-92af-d506-e063-6394a90a6518", "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": "42291-025", "generic_name": "Amlodipine Besylate", "labeler_name": "AvKARE", "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": "20230622", "listing_expiration_date": "20271231"}