Package 68071-2520-9

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 68071-2520-9
Digits Only 6807125209
Product NDC 68071-2520
Description

90 TABLET in 1 BOTTLE (68071-2520-9)

Marketing

Marketing Status
Marketed Since 2021-08-27
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": "1885021d-6fe5-9a81-e063-6394a90aba9c", "openfda": {"upc": ["0368071252095"], "unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["ca8c6ca7-79c6-5299-e053-2a95a90a790d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-2520-9)", "package_ndc": "68071-2520-9", "marketing_start_date": "20210827"}], "brand_name": "Amlodipine Besylate", "product_id": "68071-2520_1885021d-6fe5-9a81-e063-6394a90aba9c", "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": "68071-2520", "generic_name": "Amlodipine besylate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20101020", "listing_expiration_date": "20261231"}