Lortab Oral tablet 10-500mg Information - Conditions, Pregnancy, ingredients
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Lortab: Oral tablet (10-500mg)

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Most Commonly Used
Drug Image file DrugItem_1975.JPG
Lortab 10/500 Tab
UCB Pharma Inc
Pill Identification: 910  |  ucb

CVS/pharmacy Patient Statistics for Lortab: Oral tablet(10-500mg)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information

Lortab 10/500 Tablet

NDC: 504740910
  • Prescription Required
  • Federally Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Severe Pain, Moderate Pain

Sometimes used for but not FDA approved for the following conditions:
Bone Pain, Migraine, Myalgia, Arthralgia, Dental Pain, Headache

Storage Information
Protect from light
Store at controlled room temperature (between 68 and 77 degrees F)
Lortab 10/500 Tablet
Drug Image file DrugItem_1975.JPG
UCB Pharma Inc
Pill Identification: 910  |  ucb
Shape: oblong
Color: pink

Reported Side Effects for Lortab 10/500 Tablet

Red, Pimple Rash Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Lyell'S Syndrome Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Stevens-Johnson Syndrome Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Withdrawal Incidence:
>1.0%*
Severity: MODERATE
Onset: EARLY
Upset Stomach Incidence:
1.0%*
Severity: MILD
Onset: EARLY
Dry Mouth Incidence:
3.0%*
Severity: MILD
Onset: EARLY
Itching Incidence:
3.0%*
Severity: MILD
Onset: RAPID
Lightheadedness Incidence:
5.0-16.0%*
Severity: MILD
Onset: EARLY
Vomiting Incidence:
9.0-16.0%*
Severity: MILD
Onset: EARLY
Drowsiness Incidence:
9.3-15.0%*
Severity: MILD
Onset: EARLY
Addiction Incidence:
>10.0%*
Severity: MODERATE
Onset: DELAYED
Addiction Incidence:
>10.0%*
Severity: MODERATE
Onset: DELAYED
Miosis Incidence:
>10.0%*
Severity: MILD
Onset: EARLY
Elated Mood Incidence:
>10.0%*
Severity: MODERATE
Onset: EARLY
Headache Incidence:
12.0%*
Severity: MILD
Onset: EARLY
Constipation Incidence:
15.0-90.0%*
Severity: MODERATE
Onset: DELAYED
Upset Stomach Incidence:
27.0%*
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 Lortab 10/500 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 Lortab 10/500 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 Lortab 10/500 Tablet(Hydrocodone Bitartrate)
Alcohol and CNS Depressants(Hydrocodone Bitartrate)
Avoid alcohol-containing drinks while taking medicines that cause drowsiness. Using some of these drugs 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 if you are drinking alcohol-containing beverages. If you notice slurred speech, confusion, severe weakness, or difficulty breathing, contact your health care provider immediately.
Major Lifestyle Interaction
Grapefruit juice and Lortab 10/500 Tablet(Hydrocodone Bitartrate)
Grapefruit juice and Hydrocodone(Hydrocodone Bitartrate)
Side effects from Hydrocodone may get worse if you eat or drink grapefruit juice. Talk to your doctor first. Contact your doctor right away if you have slurred speech, confusion, weakness, or trouble breathing. Do not drive or operate machinery until you know how this affects you.
Moderate Lifestyle Interaction
Tobacco and Lortab 10/500 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.


Learning More About
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