Label: VERAPAMIL HYDROCHLORIDE tablet

  • NDC Code(s): 70771-1953-1, 70771-1953-5, 70771-1954-1, 70771-1954-5, view more
    70771-1955-1, 70771-1955-5
  • Packager: Zydus Lifesciences Limited
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated April 9, 2026

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    NDC 70771-1953-1 in bottles of 100 tablets

    Verapamil Hydrochloride Extended-Release Tablets, USP 120 mg

    100 Tablets

    Rx Only

    image

    NDC 70771-1954-1 in bottles of 100 tablets

    Verapamil Hydrochloride Extended-Release Tablets, USP 180 mg

    100 Tablets

    Rx Only

    image

    NDC 70771-1955-1 in bottles of 100 tablets

    Verapamil Hydrochloride Extended-Release Tablets, USP 240 mg

    100 Tablets

    Rx Only

    image
  • INGREDIENTS AND APPEARANCE
    VERAPAMIL HYDROCHLORIDE 
    verapamil hydrochloride tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1953
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE120 mg
    Inactive Ingredients
    Ingredient NameStrength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    POVIDONE K30 (UNII: U725QWY32X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    TALC (UNII: 7SEV7J4R1U)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    Product Characteristics
    ColorBROWN (Beige) Scoreno score
    ShapeOVALSize11mm
    FlavorImprint Code 61;5
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70771-1953-1100 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
    2NDC:70771-1953-5500 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21925205/21/2026
    VERAPAMIL HYDROCHLORIDE 
    verapamil hydrochloride tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1954
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE180 mg
    Inactive Ingredients
    Ingredient NameStrength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    POVIDONE K30 (UNII: U725QWY32X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    TALC (UNII: 7SEV7J4R1U)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    Product Characteristics
    ColorBROWN (Beige) Score2 pieces
    ShapeOVALSize15mm
    FlavorImprint Code 562
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70771-1954-1100 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
    2NDC:70771-1954-5500 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21925205/21/2026
    VERAPAMIL HYDROCHLORIDE 
    verapamil hydrochloride tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1955
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE240 mg
    Inactive Ingredients
    Ingredient NameStrength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    POVIDONE K30 (UNII: U725QWY32X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    TALC (UNII: 7SEV7J4R1U)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    Product Characteristics
    ColorBROWN (Beige) Score2 pieces
    ShapeOVAL (Capsule) Size18mm
    FlavorImprint Code 563
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70771-1955-1100 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
    2NDC:70771-1955-5500 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21925205/21/2026
    Labeler - Zydus Lifesciences Limited (918596198)
    Registrant - Zydus Lifesciences Limited (677605858)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zydus Lifesciences Limited677605858ANALYSIS(70771-1953, 70771-1954, 70771-1955) , MANUFACTURE(70771-1953, 70771-1954, 70771-1955)