Home > Pill Identifier > zolmitriptan 2.5 MG Disintegrating Tablet

Pill Identifier Information of zolmitriptan 2.5 MG Disintegrating Tablet

Drug Information

zolmitriptan 2.5 MG Disintegrating Tablet

Imprint: 715
Shape: C48348
Color: C48325
Ingredients: zolmitriptan
Size: 6.00
Score: 1
Rxtty: SCD
Author: Cadila Healthcare Limited
Inactive Ingredients: ANHYDROUS CITRIC ACID / ASPARTAME / COLLOIDAL SILICON DIOXIDE / CROSPOVIDONE / GELATIN / MAGNESIUM STEARATE / MANNITOL / CELLULOSE, MICROCRYSTALLINE / ORANGE / POLACRILIN POTASSIUM / SODIUM STEARYL FUMARATE>

Complete Information

  • SPL UNCLASSIFIED SECTION

  • PRINCIPAL DISPLAY PANEL

    NDC 65841-767-69 in blister pack of 6 Tablets

    Zolmitriptan Orally Disintegrating Tablets, 2.5 mg

    Rx only

    6 Tablets

    Zolmitriptan OD Tablets, 2.5 mg
  • PRINCIPAL DISPLAY PANEL

    NDC 65841-768-87 in blister pack of 3 Tablets

    Zolmitriptan Orally Disintegrating Tablets, 5 mg

    Rx only

    3 Tablets

    Zolmitritan OD Tablets, 5 mg
  • INGREDIENTS AND APPEARANCE
    ZOLMITRIPTAN 
    zolmitriptan tablet, orally disintegrating
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:65841-767
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZOLMITRIPTAN (UNII: 2FS66TH3YW) (ZOLMITRIPTAN - UNII:2FS66TH3YW) ZOLMITRIPTAN2.5 mg
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ASPARTAME (UNII: Z0H242BBR1)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)  
    GELATIN (UNII: 2G86QN327L)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MANNITOL (UNII: 3OWL53L36A)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    ORANGE (UNII: 5EVU04N5QU)  
    POLACRILIN POTASSIUM (UNII: 0BZ5A00FQU)  
    SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)  
    Product Characteristics
    ColorWHITE (WHITE/MOTTLED WHITE TO CREAM WHITE) Scoreno score
    ShapeROUND (ROUND) Size6mm
    FlavorORANGE (ORANGE) Imprint Code 715
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65841-767-0630 in 1 BOTTLE; Type 0: Not a Combination Product05/16/2013
    2NDC:65841-767-1690 in 1 BOTTLE; Type 0: Not a Combination Product05/16/2013
    3NDC:65841-767-01100 in 1 BOTTLE; Type 0: Not a Combination Product05/16/2013
    4NDC:65841-767-101000 in 1 BOTTLE; Type 0: Not a Combination Product05/16/2013
    5NDC:65841-767-861 in 1 CARTON05/16/2013
    5NDC:65841-767-696 in 1 BLISTER PACK; Type 0: Not a Combination Product
    6NDC:65841-767-7710 in 1 CARTON05/16/2013
    6NDC:65841-767-3010 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20289005/16/2013
    ZOLMITRIPTAN 
    zolmitriptan tablet, orally disintegrating
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:65841-768
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZOLMITRIPTAN (UNII: 2FS66TH3YW) (ZOLMITRIPTAN - UNII:2FS66TH3YW) ZOLMITRIPTAN5 mg
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ASPARTAME (UNII: Z0H242BBR1)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)  
    GELATIN (UNII: 2G86QN327L)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MANNITOL (UNII: 3OWL53L36A)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    ORANGE (UNII: 5EVU04N5QU)  
    POLACRILIN POTASSIUM (UNII: 0BZ5A00FQU)  
    SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)  
    Product Characteristics
    ColorWHITE (WHITE/MOTTLED WHITE TO CREAM WHITE) Scoreno score
    ShapeROUND (ROUND) Size9mm
    FlavorORANGE (ORANGE) Imprint Code 717
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65841-768-0630 in 1 BOTTLE; Type 0: Not a Combination Product05/16/2013
    2NDC:65841-768-1690 in 1 BOTTLE; Type 0: Not a Combination Product05/16/2013
    3NDC:65841-768-01100 in 1 BOTTLE; Type 0: Not a Combination Product05/16/2013
    4NDC:65841-768-101000 in 1 BOTTLE; Type 0: Not a Combination Product05/16/2013
    5NDC:65841-768-821 in 1 CARTON05/16/2013
    5NDC:65841-768-873 in 1 BLISTER PACK; Type 0: Not a Combination Product
    6NDC:65841-768-7710 in 1 CARTON05/16/2013
    6NDC:65841-768-3010 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20289005/16/2013
    Labeler - Zydus Lifesciences Limited (918596198)
    Registrant - Zydus Lifesciences Limited (918596198)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zydus Lifesciences Limited918596198ANALYSIS(65841-767, 65841-768) , MANUFACTURE(65841-767, 65841-768)
© 2026 - Pharmaguru.com. All rights reserved.