Home > Pill Identifier > venlafaxine 50 MG (as venlaxfaxine hydrochloride 56.6 MG) Oral Tablet

Pill Identifier Information of venlafaxine 50 MG (as venlaxfaxine hydrochloride 56.6 MG) Oral Tablet

Drug Information

venlafaxine 50 MG (as venlaxfaxine hydrochloride 56.6 MG) Oral Tablet

Imprint: ZC;66
Shape: C48348
Color: C48331
Ingredients: venlafaxine
Size: 8.00
Score: 2
Rxtty: SY
Author: Cadila Healthcare Limited
Inactive Ingredients: FERRIC OXIDE YELLOW / LACTOSE MONOHYDRATE / MAGNESIUM STEARATE / SODIUM STARCH GLYCOLATE TYPE A POTATO / FERRIC OXIDE RED / CELLULOSE, MICROCRYSTALLINE>

Complete Information

  • SPL UNCLASSIFIED SECTION

  • SPL MEDGUIDE

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    NDC 65841-671-01 in bottle of 100 Tablets

    Venlafaxine Hydrochloride Tablets, 25 mg

    Rx only

    100 TABLETS

     

    Venlafaxine Tablets USP, 25 mg

    NDC 65841-672-01 in bottle of 100 Tablets

    Venlafaxine Hydrochloride Tablets, 37.5 mg

    Rx only

    100 TABLETS

     

    Venlafaxine Tablets USP, 37.5 mg

    NDC 65841-673-01 in bottle of 100 Tablets

    Venlafaxine Hydrochloride Tablets, 50 mg

    Rx only

    100 TABLETS

    Venlafaxine Tablets USP, 50 mg

    NDC 65841-674-01 in bottle of 100 Tablets

    Venlafaxine Hydrochloride Tablets, 75 mg

    Rx only

    100 TABLETS

    Venlafaxine Tablets USP, 75 mg

    NDC 65841-675-01 in bottle of 100 Tablets

    Venlafaxine Hydrochloride Tablets, 100 mg

    Rx only

    100 TABLETS

    Venlafaxine Tablets USP, 100 mg
  • INGREDIENTS AND APPEARANCE
    VENLAFAXINE HYDROCHLORIDE 
    venlafaxine hydrochloride tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:65841-671
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VENLAFAXINE HYDROCHLORIDE (UNII: 7D7RX5A8MO) (VENLAFAXINE - UNII:GRZ5RCB1QG) VENLAFAXINE25 mg
    Inactive Ingredients
    Ingredient NameStrength
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    Product Characteristics
    ColorORANGE (PEACH) Score2 pieces
    ShapeROUND (ROUND) Size6mm
    FlavorImprint Code ZC;64
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65841-671-0630 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    2NDC:65841-671-1460 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    3NDC:65841-671-1690 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    4NDC:65841-671-01100 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    5NDC:65841-671-05500 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    6NDC:65841-671-101000 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07765306/13/2008
    VENLAFAXINE HYDROCHLORIDE 
    venlafaxine hydrochloride tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:65841-672
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VENLAFAXINE HYDROCHLORIDE (UNII: 7D7RX5A8MO) (VENLAFAXINE - UNII:GRZ5RCB1QG) VENLAFAXINE37.5 mg
    Inactive Ingredients
    Ingredient NameStrength
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    Product Characteristics
    ColorORANGE (PEACH) Score2 pieces
    ShapeROUND (ROUND) Size7mm
    FlavorImprint Code ZC;65
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65841-672-0630 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    2NDC:65841-672-1460 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    3NDC:65841-672-1690 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    4NDC:65841-672-01100 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    5NDC:65841-672-05500 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    6NDC:65841-672-101000 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07765306/13/2008
    VENLAFAXINE HYDROCHLORIDE 
    venlafaxine hydrochloride tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:65841-673
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VENLAFAXINE HYDROCHLORIDE (UNII: 7D7RX5A8MO) (VENLAFAXINE - UNII:GRZ5RCB1QG) VENLAFAXINE50 mg
    Inactive Ingredients
    Ingredient NameStrength
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    Product Characteristics
    ColorORANGE (PEACH) Score2 pieces
    ShapeROUND (ROUND) Size8mm
    FlavorImprint Code ZC;66
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65841-673-0630 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    2NDC:65841-673-1460 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    3NDC:65841-673-1690 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    4NDC:65841-673-01100 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    5NDC:65841-673-05500 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    6NDC:65841-673-101000 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07765306/13/2008
    VENLAFAXINE HYDROCHLORIDE 
    venlafaxine hydrochloride tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:65841-674
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VENLAFAXINE HYDROCHLORIDE (UNII: 7D7RX5A8MO) (VENLAFAXINE - UNII:GRZ5RCB1QG) VENLAFAXINE75 mg
    Inactive Ingredients
    Ingredient NameStrength
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    Product Characteristics
    ColorORANGE (PEACH) Score2 pieces
    ShapeROUND (ROUND) Size10mm
    FlavorImprint Code ZC;67
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65841-674-0630 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    2NDC:65841-674-1460 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    3NDC:65841-674-1690 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    4NDC:65841-674-01100 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    5NDC:65841-674-05500 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    6NDC:65841-674-101000 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07765306/13/2008
    VENLAFAXINE HYDROCHLORIDE 
    venlafaxine hydrochloride tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:65841-675
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VENLAFAXINE HYDROCHLORIDE (UNII: 7D7RX5A8MO) (VENLAFAXINE - UNII:GRZ5RCB1QG) VENLAFAXINE100 mg
    Inactive Ingredients
    Ingredient NameStrength
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    Product Characteristics
    ColorORANGE (PEACH) Score2 pieces
    ShapeROUND (ROUND) Size10mm
    FlavorImprint Code ZC;68
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65841-675-0630 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    2NDC:65841-675-1460 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    3NDC:65841-675-1690 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    4NDC:65841-675-01100 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    5NDC:65841-675-05500 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    6NDC:65841-675-101000 in 1 BOTTLE; Type 0: Not a Combination Product06/13/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07765306/13/2008
    Labeler - Zydus Lifesciences Limited (918596198)
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