Package 50090-6877-0

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 50090-6877-0
Digits Only 5009068770
Product NDC 50090-6877
Product ID 50090-6877_284221d6-4e43-46b1-9ddf-c6f19bfce2af
Description

90 TABLET in 1 BOTTLE (50090-6877-0)

Marketing

Marketing Status
Marketed Since 2023-12-05
Brand amlodipine besylate
Generic amlodipine besylate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "284221d6-4e43-46b1-9ddf-c6f19bfce2af", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["197361"], "spl_set_id": ["699d3ba2-a342-4e3d-b8ad-c14e0df64dfe"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6877-0)", "package_ndc": "50090-6877-0", "marketing_start_date": "20231205"}], "brand_name": "Amlodipine Besylate", "product_id": "50090-6877_284221d6-4e43-46b1-9ddf-c6f19bfce2af", "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": "50090-6877", "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": "ANDA203245", "marketing_category": "ANDA", "marketing_start_date": "20190522", "listing_expiration_date": "20261231"}