Package 50090-5059-0

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 50090-5059-0
Digits Only 5009050590
Product NDC 50090-5059
Description

90 TABLET in 1 BOTTLE (50090-5059-0)

Marketing

Marketing Status
Marketed Since 2020-05-26
Brand amlodipine besylate
Generic amlodipine besylate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1ae0dd3b-94e2-4d58-87b0-c6df923aa27e", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["197361"], "spl_set_id": ["4512feee-a09d-4244-bc03-c43193e53a0e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5059-0)", "package_ndc": "50090-5059-0", "marketing_start_date": "20200526"}], "brand_name": "Amlodipine Besylate", "product_id": "50090-5059_1ae0dd3b-94e2-4d58-87b0-c6df923aa27e", "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": "50090-5059", "generic_name": "Amlodipine besylate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}], "application_number": "ANDA078925", "marketing_category": "ANDA", "marketing_start_date": "20101020", "listing_expiration_date": "20261231"}