Package 72162-2232-1

Brand: verapamil hydrochloride

Generic: verapamil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2232-1
Digits Only 7216222321
Product NDC 72162-2232
Description

100 TABLET in 1 BOTTLE (72162-2232-1)

Marketing

Marketing Status
Marketed Since 2024-01-26
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": "d10e4b7e-6e14-40a5-9bd3-94e51e4515b8", "openfda": {"unii": ["V3888OEY5R"], "rxcui": ["897683"], "spl_set_id": ["d4a6c046-81fe-4b2a-9cb0-adb3f037eec7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2232-1)", "package_ndc": "72162-2232-1", "marketing_start_date": "20240126"}], "brand_name": "VERAPAMIL HYDROCHLORIDE", "product_id": "72162-2232_d10e4b7e-6e14-40a5-9bd3-94e51e4515b8", "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": "72162-2232", "generic_name": "VERAPAMIL HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VERAPAMIL HYDROCHLORIDE", "active_ingredients": [{"name": "VERAPAMIL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA071881", "marketing_category": "ANDA", "marketing_start_date": "20110107", "listing_expiration_date": "20261231"}