VERAPAMIL HYDROCHLORIDE

Product NDC
68788-8696
11-digit product format
687888696
Labeler code
68788
Product ID
68788-8696_dfb38dc3-25c5-472c-b723-c407be886316
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
VERAPAMIL HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA206173
Marketing category
ANDA
Marketing start
2024-06-11
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
68788-8696-168788869601100 TABLET in 1 BOTTLE (68788-8696-1) 100 tablet2024-06-11NoNoHistorical
68788-8696-36878886960330 TABLET in 1 BOTTLE (68788-8696-3) 30 tablet2024-06-11NoNoHistorical
68788-8696-96878886960990 TABLET in 1 BOTTLE (68788-8696-9) 90 tablet2024-06-11NoNoHistorical

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 TabletsPreferred Pharmaceuticals Inc.2024-06-11HUMAN PRESCRIPTION DRUG LABEL1