Home > Pill Identifier > loratadine 10 MG / pseudoephedrine sulfate 240 MG 24 HR Extended Release Tablet

Pill Identifier Information of loratadine 10 MG / pseudoephedrine sulfate 240 MG 24 HR Extended Release Tablet

Drug Information

loratadine 10 MG / pseudoephedrine sulfate 240 MG 24 HR Extended Release Tablet

Imprint: RX724
Shape: C48336
Color: C48325
Ingredients: Loratadine; Pseudoephedrine
Size: 17.00
Score: 1
Rxtty: SY
Author: Select Brand
Inactive Ingredients: CALCIUM CARBONATE / COLLOIDAL SILICON DIOXIDE / HYDROXYPROPYL CELLULOSE / HYPROMELLOSES / FERROSOFERRIC OXIDE / LACTOSE MONOHYDRATE / MAGNESIUM STEARATE / CELLULOSE, MICROCRYSTALLINE / POLYETHYLENE GLYCOLS / POVIDONE / STARCH, PREGELATINIZED CORN / PROPYLENE GLYCOL / SHELLAC / SODIUM ALGINATE / SODIUM CITRATE / TALC / TITANIUM DIOXIDE>

Complete Information

  • ACTIVE INGREDIENTS (IN EACH TABLET)

    Loratadine, USP 10 mg

    Pseudoephedrine sulfate, USP 240 mg

  • PURPOSE

    Antihistamine

    Nasal decongestant

  • USES

    • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
      • sneezing
      • itchy, watery eyes
      • runny nose
      • itching of the nose or throat
  • reduces swelling of nasal passages
  • temporarily relieves sinus congestion and pressure
  • temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies
  • temporarily restores freer breathing through the nose
  • WARNINGS

    Do not use
    • if you have ever had an allergic reaction to this product or any of its ingredients
    • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

    Ask a doctor before use if you have
    • heart disease
    • thyroid disease
    • high blood pressure
    • diabetes
    • trouble urinating due to an enlarged prostate gland
    • liver or kidney disease. Your doctor should determine if you need a different dose.

    • When using this product do not take more than directed.

    Taking more than directed may cause drowsiness.

    Stop use and ask a doctor if

    If pregnant or breast-feeding

    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 (1-800-222-1222).

  • DIRECTIONS

  • OTHER INFORMATION

  • INACTIVE INGREDIENTS

    Calcium carbonate, colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, iron oxide black, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch, propylene glycol, shellac glaze, sodium alginate, sodium citrate, talc and titanium dioxide

  • QUESTIONS?

    Call 1-800-406-7984

  • PRINCIPAL DISPLAY PANEL

    †Compare to the active ingredients of Claritin-D®24 Hour

    NDC 15127-717-05

    NON-DROWSY*

    select brand®

    Original Prescription Strength

    Allergy Relief and Nasal Decongestant

    24 Hour Formula

    Loratadine, USP 10 mg/Antihistamine

    Pseudoephedrine Sulfate, USP 240 mg/Nasal Decongestant

    Indoor & Outdoor Allergies

    Allergy & Congestion

    RELIEF OF:

    Nasal and Sinus Congestion Due to Colds or Allergies

    Sneezing; Runny Nose

    Itchy, Watery Eyes; Itchy Throat

    or Nose Due to Allergies

    5 Extended-Release Tablets

    *When taken as directed. See Drug Facts Panel.

    Distributed by: SELECT BRAND DISTRIBUTORS

    5079457/R0710

    This is the 5 count blister carton label for Select Brand Loratadine D tablets.
  • INGREDIENTS AND APPEARANCE
    LORATADINE AND PSEUDOEPHEDRINE SULFATE 
    loratadine and pseudoephedrine sulfate tablet, film coated, extended release
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15127-717
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
    PSEUDOEPHEDRINE SULFATE (UNII: Y9DL7QPE6B) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE SULFATE240 mg
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK)  
    COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    POVIDONE (UNII: FZ989GH94E)  
    STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Colorwhite (White to Off-White) Scoreno score
    ShapeCAPSULESize17mm
    FlavorImprint Code RX724
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:15127-717-1515 in 1 BLISTER PACK
    2NDC:15127-717-055 in 1 BLISTER PACK
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07655711/17/2004
    Labeler - Select Brand (043562370)
    Registrant - Ranbaxy Pharmaceuticals Inc. (937890044)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ohm Laboratories Inc.051565745manufacture(15127-717)