ACETAMINOPHEN  - acetaminophen tablet 
Preferred Pharmaceuticals, Inc

325 mg

Drug Facts

Active ingredient (in each tablet)

Acetaminophen 325 mg


Pain reliever/fever reducer


to reduce fever and for the temporary relief of minor aches and pains due to

  • headache
  • backache
  • the common cold
  • premenstrual and menstrual cramps
  • muscular aches
  • minor pain of arthritis
  • toothache

Temporarily reduces fever.


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 doses in 24 hours
  • taken with other drugs containing acetaminophen
  • adult has 3 or more alcoholic drinks everyday while using this product

Ask a doctor before use if the user has liver disease.

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.

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

Stop use and ask a doctor if

  • pain gets worse or lasts more than 10 days in adults and children
  • pain gets worse or lasts more than 5 days in children under 12 years
  • 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

Taking more than the recommended dose (overdose) may cause liver damage. 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.


Do not take more than directed.

adults and children 12 years and over
  • take 2 tablets every 4 to 6 hours while symptoms last
  • do not take more than 12 tablets in 24 hours
children 6 to 11 years
  • take 1 tablet every 4 to 6 hours while symptoms last
  • do not take more than 5 tablets in 24 hours
children under 6 years Do not use adult regular strength products in children under 6 years of age; this will provide more than the recommended dose (overdose) of acetaminophen and may cause liver damage.

Other information

  • TAMPER-EVIDENT: Each tablet is individually sealed. Do not use if blister is torn or broken.
  • store at controlled room temperature 15° - 30°C (59° - 86°F)
  • protect from moisture, heat and light

Inactive ingredients

povidone, starch, stearic acid


call 1-888-838-2872, weekdays, 8 AM - 5 PM Eastern Time

This unit dose package is not child-resistant. If dispensed for outpatient use, a child-resistant container should be utilized.

Manufactured for:
Sellersville, PA 18960
by: LNK International, Inc.
Hauppauge, NY 11788
0609REV 05 99-391
Repackaged by Preferred Pharmaceuticals, Inc
Anaheim, CA 92870


NDC 68788-0775


Repackaged By;
Preferred Pharmaceuticals, Inc
Principal Display Panel - 325 mg tablets

acetaminophen  tablet
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 68788-0775 (0182-8447)
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Acetaminophen (Acetaminophen) Acetaminophen 325 mg
Inactive Ingredients
Ingredient Name Strength
stearic acid  
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND (Bisect with flat face and beveled edge) Size 10mm
Flavor Imprint Code 44;104
# NDC Package Description Multilevel Packaging
1 68788-0775-2 20 TABLET In 1 BOTTLE None
2 68788-0775-3 30 TABLET In 1 BOTTLE None
3 68788-0775-6 60 TABLET In 1 BOTTLE None
4 68788-0775-9 90 TABLET In 1 BOTTLE None
5 68788-0775-1 100 TABLET In 1 BOTTLE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part343 01/01/2023

Labeler - Preferred Pharmaceuticals, Inc (791119022)
Name Address ID/FEI Operations
Preferred Pharmaceuticals, Inc 791119022 repack, relabel
Revised: 03/2011Preferred Pharmaceuticals, Inc