VERAPAMIL HYDROCHLORIDE
Verapamil Hydrochloride Tablets, USP These highlights do not include all the information needed to use VERAPAMIL HYDROCHLORIDE safely and effectively. See full prescribing information for VERAPAMIL HYDROCHLORIDE VERAPAMIL HYDROCHLORIDE (VERAPAMIL HYDROCHLORIDE) TABLET for ORAL use. Initial U.S. Approval:
Approved
Approval ID
a9cc4b42-184c-587e-e053-2995a90aa6d5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 6, 2020
Manufacturers
FDA
Denton Pharma, Inc. dba Northwind Pharmaceuticals
DUNS: 080355546
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 Code70934-739
Application NumberANDA071881
Product Classification
M
Marketing Category
C73584
G
Generic Name
VERAPAMIL HYDROCHLORIDE
Product Specifications
Route of AdministrationORAL
Effective DateJuly 6, 2020
FDA Product Classification
INGREDIENTS (10)
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATEInactive
Code: O7TSZ97GEP
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
MINERAL OILInactive
Code: T5L8T28FGP
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
VERAPAMIL HYDROCHLORIDEActive
Quantity: 120 mg in 1 1
Code: V3888OEY5R
Classification: ACTIB
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
HYPROMELLOSE 2910 (6 MPA.S)Inactive
Code: 0WZ8WG20P6
Classification: IACT