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Pill Identifier Information of APAP 325 MG Oral Tablet

Drug Information

APAP 325 MG Oral Tablet

Imprint: AP;012
Shape: C48348
Color: C48325
Ingredients: Acetaminophen
Size: 8.00
Score: 1
Rxtty: SY
Author: Advance Pharmaceutical Inc.
Inactive Ingredients: POVIDONE / STARCH, CORN / SODIUM STARCH GLYCOLATE TYPE A POTATO / STEARIC ACID>

Complete Information

  • Active Ingredient

    (in each tablet)

    Acetaminophen 325 mg

  • Purpose

    Pain Reliever / Fever Reducer

  • Uses

    temporarily reduces fever and relieves minor aches and pains caused by

    • common cold
    • headache
    • toothache
    • muscular aches
    • premenstrual and menstrual cramps
  • Warnings

    Liver warning: this product contains acetaminophen. Severe liver damage may occur if

    • adult takes more than 12 tablets in 24 hours, which is the maximum daily amount
    • child takes more than 5 tablets in 24 hours, which is the maximum daily amount
    • taken with other drugs containing acetaminophen
    • adult has 3 or more alcoholic drinks every day while using this product

    do not use with any other drug containing acetaminophen (prescription or non prescription).        If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

    Ask a doctor before use if the user has liver disease

    Ask a doctor or pharmacist before use if the user is taking the blood thinning drug warfarin

    Stop use and ask a doctor if

    • adult’s pain gets worse or lasts more than 10 days
    • child’s pain gets worse or lasts more than 5 days
    • fever gets worse or lasts more than 3 days
    • redness or swelling is present
    • any new symptoms appear

    • 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. Prompt medical attention is critical for adults as well as for children, even if you do not notice any signs or symptoms.

  • Directions

    adults and children 12 years and over 1-2 tablets every 4 hours or 2-3 tablets every 6 hours while symptoms last, not more than 12 tablets in 24 hours
    children 6 to 11 years 1 tablet every 4 hours while symptoms last, not more than 5 tablets in 24 hours
    children under 6 yearsask a doctor
  • Other Information

    • store at 15-30 °C (59-86 °F)

    For Bulk package: This is a bulk package, dispense contents with a child-resistant closure in a tight, light resistant container as defined in the USP.

  • Inactive Ingredients

    polyvinylpyrrolidone, pregelatinized corn starch, sodium starch glycolate, stearic acid

  • Questions or Comments

    TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

    Manufactured by: Advance Pharmaceutical, Inc. Holtsville, NY 11742

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    1d2e4055-figure-01

    1d2e4055-figure-02

    1d2e4055-figure-03

    NDC: 17714-012-01 – 100 COUNT

    NDC: 17714-012-10 – 1000 COUNT

  • INGREDIENTS AND APPEARANCE
    ACETAMINOPHEN 
    acetaminophen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17714-012
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
    Inactive Ingredients
    Ingredient NameStrength
    POVIDONE (UNII: FZ989GH94E)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize8mm
    FlavorImprint Code AP;012
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17714-012-01100 in 1 BOTTLE; Type 0: Not a Combination Product02/05/1989
    2NDC:17714-012-101000 in 1 BOTTLE; Type 0: Not a Combination Product02/05/1989
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34302/05/1989
    Labeler - Advance Pharmaceutical Inc. (078301063)
    Registrant - Advance Pharmaceutical Inc. (078301063)
    Establishment
    NameAddressID/FEIBusiness Operations
    Advance Pharmaceutical Inc.078301063manufacture(17714-012)