Package 50090-5355-0

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 50090-5355-0
Digits Only 5009053550
Product NDC 50090-5355
Product ID 50090-5355_d8ecdea1-29fa-45d7-b0aa-72f7466ce915
Description

90 TABLET in 1 BOTTLE (50090-5355-0)

Marketing

Marketing Status
Marketed Since 2020-11-11
Brand amlodipine besylate
Generic amlodipine besylate
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d8ecdea1-29fa-45d7-b0aa-72f7466ce915", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["91e11ca6-05fb-47be-bd40-f8649a35d47d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5355-0)", "package_ndc": "50090-5355-0", "marketing_start_date": "20201111"}], "brand_name": "Amlodipine Besylate", "product_id": "50090-5355_d8ecdea1-29fa-45d7-b0aa-72f7466ce915", "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": "50090-5355", "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": "10 mg/1"}], "application_number": "ANDA078043", "marketing_category": "ANDA", "marketing_start_date": "20180815", "listing_expiration_date": "20261231"}