DrugCite

ACETAMINOPHEN - acetaminophen tablet, film coated, extended release 
Chain Drug Marketing Association Inc.

Drug Facts

ACTIVE INGREDIENT (IN EACH CAPLET)

Acetaminophen USP, 650 mg

PURPOSE

Pain reliever/fever reducer

USES

  • temporarily relieves minor aches and pains due to:
    • minor pain of arthritis
    • muscular aches
    • backache
    • headache
    • toothache
    • the common cold
    • premenstrual and menstrual cramps
  • temporarily reduces fever

WARNINGS

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take

  • more than 6 caplets in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

Do not use

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • if you are allergic to acetaminophen or any of the inactive ingredients in this product.

Ask a doctor before use if you have

Liver disease.

Ask a doctor or pharmacist before use if you are

Taking the blood thinning drug warfarin.

Stop use and ask a doctor if

  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days
  • new symptoms occur
  • redness or swelling is present

These could be signs of a serious condition.

If pregnant or breast-feeding

Ask a health professional before use.

Keep out of reach of children.

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

DIRECTIONS

  • do not take more than directed (see overdose warning)
    adults take 2 caplets every 8 hours with water
    swallow whole - do not crush, chew, split or dissolve
    do not take more than 6 caplets in 24 hours
    do not use for more than 10 days unless directed by a doctor
    under 18 years of age ask a doctor

OTHER INFORMATION

  • store at 20 - 25° C (68 - 77° F). Avoid excessive heat 40° C (104° F).
  • see end panel for batch number and expiration date
  • TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL IS BROKEN OR MISSING FROM BOTTLE.

INACTIVE INGREDIENTS

Croscarmellose sodium, hypromellose, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch, propylene glycol, sodium lauryl sulfate, stearic acid, titanium dioxide

QUESTIONS?

Call 1-800-406-7984

PRINCIPAL DISPLAY PANEL

QC QUALITY CHOICE®

NDC 63868-089-01

Compare to the active ingredient in Tylenol®Arthritis Pain

Lasts Up To 8 Hours

ARTHRITIS PAIN RELIEF

Acetaminophen

See New Warnings Information

Extended-Release Tablets, USP 650 mg

Pain Reliever/Fever Reducer

For the Temporary Relief

of Minor Arthritis Pain

Use only as directed.

DO NOT USE WITH OTHER MEDICINES CONTAINING ACETAMINOPHEN

THIS PACKAGE FOR HOUSEHOLDS WITHOUT YOUNG CHILDREN

EASY TO OPEN BOTTLE

100 CAPLETS*

650 mg EACH

(*capsule-shaped tablets)

©DISTRIBUTED BY QUALITY CHOICE

5095169/R0512

This is the 100 count bottle carton label for Quality Choice Acetaminophen extended-release tablets, USP 650 mg (APAP Arthritis).


ACETAMINOPHEN 
acetaminophen  tablet, film coated, extended release
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 63868-089
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN 650 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM  
HYPROMELLOSES  
MAGNESIUM STEARATE  
CELLULOSE, MICROCRYSTALLINE  
POVIDONE  
STARCH, PREGELATINIZED CORN  
PROPYLENE GLYCOL  
SODIUM LAURYL SULFATE  
STEARIC ACID  
TITANIUM DIOXIDE  
Product Characteristics
Color white Score no score
Shape OVAL (Capsule shaped) Size 19mm
Flavor Imprint Code cor116
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 63868-089-50 50 TABLET In 1 BOTTLE None
2 63868-089-01 100 TABLET In 1 BOTTLE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076200 04/30/2002

Labeler - Chain Drug Marketing Association Inc. (011920774)
Registrant - Ranbaxy Pharmaceuticals Inc. (937890044)
Establishment
Name Address ID/FEI Operations
Ohm Laboratories Inc. 184769029 manufacture
Revised: 10/2012Chain Drug Marketing Association Inc.