Package 50090-7311-1

Brand: verapamil hydrochloride

Generic: verapamil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7311-1
Digits Only 5009073111
Product NDC 50090-7311
Description

90 TABLET in 1 BOTTLE (50090-7311-1)

Marketing

Marketing Status
Marketed Since 2024-10-14
Brand verapamil hydrochloride
Generic verapamil hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6affb2d0-1b92-4ac8-80fa-cac7807a60a3", "openfda": {"unii": ["V3888OEY5R"], "rxcui": ["897659"], "spl_set_id": ["0b00ec93-0bb3-4181-a6ef-45206f0621f7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7311-1)", "package_ndc": "50090-7311-1", "marketing_start_date": "20241014"}], "brand_name": "VERAPAMIL HYDROCHLORIDE", "product_id": "50090-7311_6affb2d0-1b92-4ac8-80fa-cac7807a60a3", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Cytochrome P450 3A4 Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]"], "product_ndc": "50090-7311", "generic_name": "VERAPAMIL HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VERAPAMIL HYDROCHLORIDE", "active_ingredients": [{"name": "VERAPAMIL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA206173", "marketing_category": "ANDA", "marketing_start_date": "20230102", "listing_expiration_date": "20261231"}