Package 82804-164-90

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 82804-164-90
Digits Only 8280416490
Product NDC 82804-164
Description

90 TABLET in 1 BOTTLE (82804-164-90)

Marketing

Marketing Status
Marketed Since 2024-11-06
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": "f18148f9-42b2-43dc-9cf8-212d9121dc5f", "openfda": {"upc": ["0382804164905"], "unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["f18148f9-42b2-43dc-9cf8-212d9121dc5f"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-164-90)", "package_ndc": "82804-164-90", "marketing_start_date": "20241106"}], "brand_name": "Amlodipine Besylate", "product_id": "82804-164_f18148f9-42b2-43dc-9cf8-212d9121dc5f", "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": "82804-164", "generic_name": "Amlodipine Besylate", "labeler_name": "Proficient Rx LP", "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"}