NDC 70518-0605

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 Remedyrepack Inc.. The primary component is Verapamil Hydrochloride.

Product ID70518-0605_7fae313f-4db5-4a10-e053-2a91aa0a63aa
NDC70518-0605
Product TypeHuman Prescription Drug
Proprietary Nameverapamil hydrochloride
Generic NameVerapamil Hydrochloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2017-07-03
Marketing CategoryANDA / ANDA
Application NumberANDA090700
Labeler NameREMEDYREPACK INC.
Substance NameVERAPAMIL HYDROCHLORIDE
Active Ingredient Strength180 mg/1
Pharm ClassesP-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70518-0605-0

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-0605-0)
Marketing Start Date2017-07-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-0605-1 [70518060501]

verapamil hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090700
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-07-31

NDC 70518-0605-0 [70518060500]

verapamil hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090700
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-07-03

Drug Details

Active Ingredients

IngredientStrength
VERAPAMIL HYDROCHLORIDE180 mg/1

OpenFDA Data

SPL SET ID:ce9ab27a-e03b-4e40-a0e0-b586cd75dead
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 897640

    • Pharmacological Class

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