Ultracet Oral Tablet 37.5-325Mg Drug Medication Dosage Information
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Ultracet: Oral tablet (37.5-325mg)

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Drug Image file DrugItem_12627.JPG
Ultracet 37.5mg-325mg Tablet
Janssen Pharmaceuticals, Inc, formerly Pricara, a Division of Ortho-McNeil-Janssen Pharmaceuticals, Inc
Pill Identification: O-M  |  650

What is this Medicine?

ACETAMINOPHEN; TRAMADOL (a set a MEE noe fen; TRA ma dole) is a pain reliever. It is used to treat short term moderate pain.

CVS Pharmacy Patient Statistics for Ultracet: Oral tablet(37.5-325mg)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information
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Ultracet 37.5mg-325mg Tablet

NDC: 504580650
  • Prescription Required
  • Federally Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Moderate Pain

Sometimes used for but not FDA approved for the following conditions:
Diabetic Neuropathy

Storage Information
Store at 77 degrees F; excursions permitted to 59-86 degrees F
Ultracet 37.5mg-325mg Tablet
Drug Image file DrugItem_12627.JPG
Janssen Pharmaceuticals, Inc, formerly Pricara, a Division of Ortho-McNeil-Janssen Pharmaceuticals, Inc
Pill Identification: O-M  |  650
Shape: oblong
Color: yellow

Reported Side Effects for Ultracet 37.5mg-325mg Tablet

Excessive Mucle Tone Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Hallucinations Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Emotional Lability Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Chills Incidence:
<1.0%*
Severity: MILD
Onset: RAPID
Chest Pain Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Incoordination Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Loss Of Memory Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Fainting Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Muscle Cramps Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Withdrawal Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Weight Loss Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Rapid Heart Rate Incidence:
<1.0%*
Severity: MODERATE
Onset: RAPID
Paresthesias Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Paranoia Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Rapid Heart Rate Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Nightmares Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Melena Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Impotence (erectile Dysfunction) Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Migraine Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Low Blood Pressure Incidence:
<1.0%*
Severity: MODERATE
Onset: RAPID
High Blood Pressure Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Shortness Of Breath Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Depression Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Anemia Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Ringing In Ears Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Retaining Urine Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Balance Problems Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Difficulty Swallowing Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Decreased Urination Incidence:
<1.0%*
Severity: SEVERE
Onset: EARLY
Nervousness Incidence:
>1.0%*
Severity: MILD
Onset: DELAYED
Stomach Pain Incidence:
>1.0%*
Severity: MILD
Onset: EARLY
Skin Rash Incidence:
>1.0%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
>1.0%*
Severity: MILD
Onset: EARLY
Shaking Incidence:
>1.0%*
Severity: MILD
Onset: EARLY
Vomiting Incidence:
>1.0%*
Severity: MILD
Onset: EARLY
Tired Incidence:
>1.0%*
Severity: MILD
Onset: EARLY
Gas Incidence:
>1.0%*
Severity: MILD
Onset: EARLY
Headache Incidence:
>1.0%*
Severity: MILD
Onset: EARLY
Elated Mood Incidence:
>1.0%*
Severity: MODERATE
Onset: EARLY
Hot Flashes Incidence:
>1.0%*
Severity: MODERATE
Onset: EARLY
Weakness Incidence:
>1.0%*
Severity: MILD
Onset: DELAYED
Confusion Incidence:
>1.0%*
Severity: MODERATE
Onset: EARLY
Itching Incidence:
2.0%*
Severity: MILD
Onset: RAPID
Dry Mouth Incidence:
2.0%*
Severity: MILD
Onset: EARLY
Inability To Sleep Incidence:
2.0%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
3.0%*
Severity: MILD
Onset: EARLY
Lightheadedness Incidence:
3.0%*
Severity: MILD
Onset: EARLY
Decreased Appetite Incidence:
3.0%*
Severity: MILD
Onset: DELAYED
Loose Stools Incidence:
3.0%*
Severity: MILD
Onset: EARLY
Excessive Sweating Incidence:
4.0%*
Severity: MILD
Onset: DELAYED
Constipation Incidence:
6.0%*
Severity: MODERATE
Onset: DELAYED
Drowsiness Incidence:
6.0%*
Severity: MILD
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Daily Life Interactions for Ultracet 37.5mg-325mg Tablet

Elements of your daily lifestyle may have an effect on the medications you are taking. Drug interactions can result in unwanted side effects, reduce the effectiveness of your medicine or possibly increase the action of a particular medicine.

Major Lifestyle Interaction
Alcohol and Ultracet 37.5mg-325mg Tablet(Acetaminophen)
Alcohol and Acetaminophen(Acetaminophen)
Patients who drink more than 3 alcoholic drinks a day and take acetaminophen are at increased risk of developing liver side effects. Avoid alcoholic drinks if you are taking acetaminophen on a regular basis.
Major Lifestyle Interaction
Alcohol and Ultracet 37.5mg-325mg Tablet(Tramadol Hydrochloride)
Alcohol and CNS Depressants(Tramadol Hydrochloride)
Avoid alcohol-containing drinks while taking this medicine. Using this drug along with alcohol can lead to serious side effects. You may feel drowsy or more tired when taking these drugs together. Do not drive or operate machinery until you know how this drug affects you, and especially if you are drinking alcohol-containing beverages. If you notice slurred speech, confusion, severe weakness, or difficulty breathing, contact your health care provider immediately.
Moderate Lifestyle Interaction
Tobacco and Ultracet 37.5mg-325mg Tablet(Acetaminophen)
Tobacco and Acetaminophen(Acetaminophen)
If you are a tobacco smoker, use of Acetaminophen can increase the risk of liver side effects. Immediately tell your doctor if you get severe abdominal pain, nausea, vomiting, or yellowing of the skin. Do not exceed 4 g acetaminophen/day in adults. Tell your doctor if Acetaminophen does not help your headache or other pain. Tobacco smoke may reduce the effectiveness of Acetaminophen.
Pregnancy & Lactation Information
FIRST Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

SECOND Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

THIRD Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

Lactation

Caution - Not enough information is available to rule out harm to infants when this drug is taken by nursing mothers.


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