VERAPAMIL HYDROCHLORIDE

Product NDC
71335-2375
11-digit product format
713352375
Labeler code
71335
Product ID
71335-2375_3b87a0c6-ec50-4d5a-b153-fcae02be4505
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
VERAPAMIL HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
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
71335-2375-17133523750130 TABLET in 1 BOTTLE (71335-2375-1) 30 tablet2024-07-08NoNoHistorical
71335-2375-27133523750290 TABLET in 1 BOTTLE (71335-2375-2) 90 tablet2024-07-08NoNoHistorical
71335-2375-371335237503100 TABLET in 1 BOTTLE (71335-2375-3) 100 tablet2024-07-08NoNoHistorical
71335-2375-47133523750460 TABLET in 1 BOTTLE (71335-2375-4) 60 tablet2024-07-08NoNoHistorical
71335-2375-57133523750510 TABLET in 1 BOTTLE (71335-2375-5) 10 tablet2024-07-08NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
VERAPAMIL HYDROCHLORIDE EXTENDED-RELEASE TABLETS USP Extended Release Film Coated TabletsBryant Ranch Prepack2024-07-08HUMAN PRESCRIPTION DRUG LABEL1