Home > Pill Identifier > Fexofenadine hydrochloride 180 MG Oral Tablet

Pill Identifier Information of Fexofenadine hydrochloride 180 MG Oral Tablet

Drug Information

Fexofenadine hydrochloride 180 MG Oral Tablet

Imprint: 194;R
Shape: C48345
Color: C48328
Ingredients: fexofenadine
Size: 7.00
Score: 1
Rxtty: SCD
Author: Physicians Total Care, Inc.
Inactive Ingredients: SILICON DIOXIDE / CROSCARMELLOSE SODIUM / magnesium stearate / mannitol / POWDERED CELLULOSE / FD&C RED NO. 40 / HYPROMELLOSE 2910 (6 MPA.S) / FERRIC OXIDE BLACK / polyethylene glycol 400 / TITANIUM DIOXIDE / STARCH, CORN>

Complete Information

  • Active ingredient(s)

    Fexofenadine HCl USP, 180 mg

  • Purpose

    Antihistamine

  • Use(s)

    temporarily relieves these symptoms due to hay fever or otherupper respiratory allergies:

    • runny nose
    • itchy, watery eys
    • sneezing
    • itching of the nose or Throad



  • Warnings

    Do not use

    if you have ever had an allergic reaction to this product or any of its ingredients.

    Ask a doctor before use if

    you have kidney disease. Your doctorshould determine if you need a different dose.

    When using this product

    do not take more than directed

    • do not take at the same time as aluminum or magnesium antacids
    • do not take with fruit juices (see Directions)

    Stop use and ask doctor if

    Allergy

    an allergic reaction to this product occurs. Seek medical help right away.

    Pregnancy/Breastfeeding

    ask a health professional before use.

    Keep out of reach of children

    In case of  overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    adults and children 12 years of age and over         take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours
    children under 12 years of agedo not use
    Adults 65 years of age  and olderask a doctor
    consumers with kidney diseaseask a doctor
  • Other information

    safety sealed: do not use if carton is opened or if individual blister units are torn or opened.

  • Storage

    store between 20° - 25°C (68° - 77°F)

    protect from excessive moisture

  • Inactive ingredients

    colloidal silicon dioxide, corn starch, croscarmellose sodium, magnesium stearate, mannitol, and powdered cellulose, opadry pink 03B54504 containing FD&C Red no. 40, hypromellose, iron oxide black, polyethylene glycol and titanium dioxide.

  • Questions

    call toll-free 1-888-375-3784

    Manufactured by:

    Dr. Reddy’s Laboratories Louisiana LLC,

    8800 Line Ave Shreveport, LA, 71106. 

    OR

    Manufactured by:

    Dr. Reddy’s Laboratories Limited

    Bachepalli - 502 325 INDIA

    Additional barcode labeling by:
    Physicians Total Care, Inc.
    Tulsa, OK      74146

  • Principal Display Panel

    Fexofenadine HCl USP, 180 mg

    NDC 54868-6289-0

    image of package label

  • INGREDIENTS AND APPEARANCE
    FEXOFENADINE HYDROCHLORIDE 
    fexofenadine hydrochloride tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54868-6289(NDC:55111-784)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Fexofenadine Hydrochloride (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V) Fexofenadine Hydrochloride180 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    magnesium stearate (UNII: 70097M6I30)  
    mannitol (UNII: 3OWL53L36A)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
    FERRIC OXIDE BLACK (UNII: XM0M87F357)  
    polyethylene glycol 400 (UNII: B697894SGQ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    ColorPINKScoreno score
    ShapeOVALSize7mm
    FlavorImprint Code 194;R
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54868-6289-030 in 1 BOTTLE
    2NDC:54868-6289-190 in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07650207/27/2011
    Labeler - Physicians Total Care, Inc. (194123980)
    Establishment
    NameAddressID/FEIBusiness Operations
    Physicians Total Care, Inc.194123980relabel, repack
© 2026 - Pharmaguru.com. All rights reserved.