Package 50090-6809-0

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 50090-6809-0
Digits Only 5009068090
Product NDC 50090-6809
Description

90 TABLET in 1 BOTTLE (50090-6809-0)

Marketing

Marketing Status
Marketed Since 2023-11-07
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": "3cd06b21-b774-4951-97e2-abcbf1256e49", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["5a67bbdc-ac1f-4778-bbdc-929df140b7f5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6809-0)", "package_ndc": "50090-6809-0", "marketing_start_date": "20231107"}], "brand_name": "Amlodipine Besylate", "product_id": "50090-6809_3cd06b21-b774-4951-97e2-abcbf1256e49", "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": "50090-6809", "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": "ANDA203245", "marketing_category": "ANDA", "marketing_start_date": "20190522", "listing_expiration_date": "20261231"}