Package 51655-586-52

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 51655-586-52
Digits Only 5165558652
Product NDC 51655-586
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-586-52)

Marketing

Marketing Status
Marketed Since 2023-01-03
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": "494ef4e0-5041-c0ae-e063-6394a90a3081", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["f32bb322-68d7-a4ca-e053-2995a90aa7b0"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-586-52)", "package_ndc": "51655-586-52", "marketing_start_date": "20230103"}], "brand_name": "Amlodipine Besylate", "product_id": "51655-586_494ef4e0-5041-c0ae-e063-6394a90a3081", "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": "51655-586", "generic_name": "Amlodipine besylate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}], "application_number": "ANDA078925", "marketing_category": "ANDA", "marketing_start_date": "20230103", "listing_expiration_date": "20271231"}