NDC 68462-260

verapamil hydrochloride

Verapamil Hydrochloride

verapamil hydrochloride is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Glenmark Pharmaceuticals Inc., Usa. The primary component is Verapamil Hydrochloride.

Product ID68462-260_032f2cc1-8c06-4297-b7c1-06bb96b18805
NDC68462-260
Product TypeHuman Prescription Drug
Proprietary Nameverapamil hydrochloride
Generic NameVerapamil Hydrochloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2009-09-17
Marketing CategoryANDA / ANDA
Application NumberANDA078906
Labeler NameGlenmark Pharmaceuticals Inc., USA
Substance NameVERAPAMIL HYDROCHLORIDE
Active Ingredient Strength240 mg/1
Pharm ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 68462-260-01

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-260-01)
Marketing Start Date2009-09-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68462-260-30 [68462026030]

verapamil hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078906
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-09-17

NDC 68462-260-05 [68462026005]

verapamil hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078906
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-09-17

NDC 68462-260-10 [68462026010]

verapamil hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078906
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-09-17

NDC 68462-260-90 [68462026090]

verapamil hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078906
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-09-17

NDC 68462-260-01 [68462026001]

verapamil hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078906
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-09-17

Drug Details

Active Ingredients

IngredientStrength
VERAPAMIL HYDROCHLORIDE240 mg/1

OpenFDA Data

SPL SET ID:ba1bf1ae-9347-4d17-998b-14bf7b5984ce
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 897640
  • 897649
  • 897659
    • UPC Code
  • 0368462292013
  • 0368462293010
  • 0368462260012

    • Pharmacological Class

    • P-Glycoprotein Inhibitors [MoA]
    • Calcium Channel Antagonists [MoA]
    • Calcium Channel Blocker [EPC]
    • Cytochrome P450 3A4 Inhibitors [MoA]
    • Cytochrome P450 3A Inhibitors [MoA]

    Medicade Reported Pricing

    68462026005 VERAPAMIL ER 240 MG TABLET

    Pricing Unit: EA | Drug Type:

    68462026001 VERAPAMIL ER 240 MG TABLET

    Pricing Unit: EA | Drug Type: