VERAPAMIL HYDROCHLORIDE

Product NDC
75834-320
11-digit product format
758340320
Labeler code
75834
Product ID
75834-320_ebbb0dad-ab4d-4d6c-aebb-d65e2dd08c28
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
VERAPAMIL HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Nivagen Pharmaceuticals, Inc.
Application
ANDA206173
Marketing category
ANDA
Marketing start
2023-01-02
Substance
VERAPAMIL HYDROCHLORIDE
Active strength
120 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
V3888OEY5RVERAPAMIL HYDROCHLORIDE152-11-4VERAPAMIL HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
75834-320-0175834032001100 TABLET in 1 BOTTLE (75834-320-01) 100 tablet2023-01-02NoNoHistorical
75834-320-0575834032005500 TABLET in 1 BOTTLE (75834-320-05) 500 tablet2023-01-02NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
VERAPAMIL HYDROCHLORIDE EXTENDED-RELEASE TABLETS USP Extended Release Film Coated TabletsPreferred Pharmaceuticals Inc.2025-10-07HUMAN PRESCRIPTION DRUG LABEL2
VERAPAMIL HYDROCHLORIDE EXTENDED-RELEASE TABLETS USP Extended Release Film Coated TabletsA-S Medication Solutions2024-10-16Human Prescription Drug Label1
VERAPAMIL HYDROCHLORIDE EXTENDED-RELEASE TABLETS USP Extended Release Film Coated TabletsBryant Ranch Prepack2024-07-08HUMAN PRESCRIPTION DRUG LABEL1
VERAPAMIL HYDROCHLORIDE EXTENDED-RELEASE TABLETS USP Extended Release Film Coated TabletsPreferred Pharmaceuticals Inc.2024-06-11HUMAN PRESCRIPTION DRUG LABEL1
VERAPAMIL HYDROCHLORIDE EXTENDED-RELEASE TABLETS USP Extended Release Film Coated TabletsNuCare Pharmaceuticals,Inc.2023-08-04HUMAN PRESCRIPTION DRUG LABEL1
VERAPAMIL HYDROCHLORIDE EXTENDED-RELEASE TABLETS USP Extended Release Film Coated TabletsNivagen Pharmaceuticals, Inc.2022-12-18Human Prescription Drug Label5