Package 71610-539-60

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 71610-539-60
Digits Only 7161053960
Product NDC 71610-539
Product ID 71610-539_882a3c50-8604-4230-aeb5-9b9df2f02a15
Description

90 TABLET in 1 BOTTLE, PLASTIC (71610-539-60)

Marketing

Marketing Status
Marketed Since 2021-04-07
Brand amlodipine besylate
Generic amlodipine besylate
Sample Package No

Linked Drug Pages (1)

Amlodipine Besylate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "882a3c50-8604-4230-aeb5-9b9df2f02a15", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["197361"], "spl_set_id": ["afcffa7b-03b7-499a-b50c-37b0e28c7737"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71610-539-60)", "package_ndc": "71610-539-60", "marketing_start_date": "20210407"}], "brand_name": "Amlodipine Besylate", "product_id": "71610-539_882a3c50-8604-4230-aeb5-9b9df2f02a15", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "71610-539", "generic_name": "Amlodipine Besylate", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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"}