Verapamil Hydrochloride
VERAPAMIL HCl EXTENDED-RELEASE TABLETS USPRx only
Approved
Approval ID
887b91f5-f117-47e6-8d59-87ac61d17175
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 20, 2010
Manufacturers
FDA
Blenheim Pharmacal, Inc.
DUNS: 171434587
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Verapamil Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code10544-541
Application NumberANDA073568
Product Classification
M
Marketing Category
C73584
G
Generic Name
Verapamil Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateAugust 20, 2010
FDA Product Classification
INGREDIENTS (10)
VERAPAMIL HYDROCHLORIDEActive
Quantity: 240 mg in 1 1
Code: V3888OEY5R
Classification: ACTIB
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
HYPROMELLOSEInactive
Code: 3NXW29V3WO
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
HYDROXYPROPYL CELLULOSEInactive
Code: RFW2ET671P
Classification: IACT
SODIUM ALGINATEInactive
Code: C269C4G2ZQ
Classification: IACT
POVIDONEInactive
Code: FZ989GH94E
Classification: IACT
POLYETHYLENE GLYCOLInactive
Code: 3WJQ0SDW1A
Classification: IACT