Reprexain Oral Tablet 10-200Mg Drug Medication Dosage Information
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Reprexain: Oral tablet (10-200mg)

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Drug Image file DrugItem_17483.JPG
Reprexain 10mg-200mg Tab
Exeltis, USA formerly Quinnova Pharmceuticals
Pill Identification: IP 117 
Drug Image file default-drug-image.png
Reprexain 10mg-200mg Tab

CVS/pharmacy Patient Statistics for Reprexain: Oral tablet(10-200mg)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information
Select a Medication

Reprexain 10mg-200mg Tablet

NDC: 237100902
  • Prescription Required
  • Federally Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Myalgia, Arthralgia, Moderate Pain

Sometimes used for but not FDA approved for the following conditions:
Bone Pain, Dental Pain

Storage Information
Store between 68 to 77 degrees F, excursions permitted 59 to 86 degrees F
Reprexain 10mg-200mg Tablet
Drug Image file DrugItem_17483.JPG
Exeltis, USA formerly Quinnova Pharmceuticals
Pill Identification: IP 117 
Shape: round
Color: yellow

Reported Side Effects for Reprexain 10mg-200mg Tablet

Glycosuria Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Inflamed Tongue Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Elated Mood Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Elevated Hepatic Enzymes Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Metallic Taste Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Confusion Incidence:
<3.0%*
Severity: MODERATE
Onset: EARLY
Weakness Incidence:
<3.0%*
Severity: MILD
Onset: DELAYED
Infection Incidence:
<3.0%*
Severity: MILD
Onset: DELAYED
Difficulty Swallowing Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Weight Loss Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Visual Impairment Incidence:
<1.0%*
Severity: SEVERE
Onset: EARLY
Rapid Heart Rate Incidence:
<1.0%*
Severity: MODERATE
Onset: RAPID
Rhinitis Incidence:
<3.0%*
Severity: MILD
Onset: EARLY
Skin Rash Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Photosensitivity Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Paresthesias Incidence:
<3.0%*
Severity: MILD
Onset: DELAYED
Rapid Heart Rate Incidence:
<3.0%*
Severity: MODERATE
Onset: EARLY
Mouth Sores Incidence:
<3.0%*
Severity: MODERATE
Onset: DELAYED
Melena Incidence:
<3.0%*
Severity: MODERATE
Onset: DELAYED
Decreased Sexual Desire Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Impotence (erectile Dysfunction) Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Excessive Mucle Tone Incidence:
<3.0%*
Severity: MODERATE
Onset: DELAYED
Hoarseness Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Hiccups Incidence:
<3.0%*
Severity: MILD
Onset: EARLY
Muscle Pain Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Low Blood Pressure Incidence:
<1.0%*
Severity: MODERATE
Onset: RAPID
Inflamed Stomach Incidence:
<3.0%*
Severity: MODERATE
Onset: DELAYED
Joint Pain Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Fever Incidence:
<3.0%*
Severity: MILD
Onset: EARLY
Throat Inflammation Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Shortness Of Breath Incidence:
<3.0%*
Severity: MODERATE
Onset: EARLY
Bladder Infection Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Depression Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Distressed Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Dry Eyes Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Balance Problems Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Hives Incidence:
<1.0%*
Severity: MILD
Onset: RAPID
Retaining Urine Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Uncontrolled Urination Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Shaking Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Ringing In Ears Incidence:
<3.0%*
Severity: MILD
Onset: DELAYED
Sinus Infection Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Decreased Appetite Incidence:
<3.0%*
Severity: MILD
Onset: DELAYED
Sore Throat Incidence:
<3.0%*
Severity: MILD
Onset: DELAYED
Nervousness Incidence:
3.0-9.0%*
Severity: MILD
Onset: DELAYED
Loose Stools Incidence:
3.0-9.0%*
Severity: MILD
Onset: EARLY
Swelling Incidence:
3.0-9.0%*
Severity: MODERATE
Onset: DELAYED
Gas Incidence:
3.0-9.0%*
Severity: MILD
Onset: EARLY
Itching Incidence:
3.0-9.0%*
Severity: MILD
Onset: RAPID
Vomiting Incidence:
3.0-9.0%*
Severity: MILD
Onset: EARLY
Dry Mouth Incidence:
3.0-9.0%*
Severity: MILD
Onset: EARLY
Stomach Pain Incidence:
3.0-9.0%*
Severity: MILD
Onset: EARLY
Addiction Incidence:
>10.0%*
Severity: MODERATE
Onset: DELAYED
Addiction Incidence:
>10.0%*
Severity: MODERATE
Onset: DELAYED
Upset Stomach Incidence:
12.0%*
Severity: MILD
Onset: EARLY
Lightheadedness Incidence:
14.0%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
21.0%*
Severity: MILD
Onset: EARLY
Drowsiness Incidence:
22.0%*
Severity: MILD
Onset: EARLY
Constipation Incidence:
22.0%*
Severity: MODERATE
Onset: DELAYED
Headache 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 Reprexain 10mg-200mg 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 Reprexain 10mg-200mg Tablet(Hydrocodone Bitartrate)
Alcohol and CNS Depressants(Hydrocodone Bitartrate)
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.
Major Lifestyle Interaction
Grapefruit juice and Reprexain 10mg-200mg 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.
Major Lifestyle Interaction
Alcohol and Reprexain 10mg-200mg Tablet(Ibuprofen)
Alcohol and Nonsteroidal antiinflammatory drugs (systemic)(Ibuprofen)
Side effects from this drug may get worse if you drink alcohol-containing drinks. If you have persistent stomach upset, vomit blood or what looks like coffee grounds, or have black, tarry stools, contact your health care provider immediately. It is best to limit or avoid alcohol containing drinks while taking this drug, even with short term use. Many non-prescription products for headaches, pain, arthritis, or sinus pain contain drugs that may cause stomach problems along with alcohol; closely read labels before taking any medicines with alcohol-containing drinks.
Moderate Lifestyle Interaction
Tobacco and Reprexain 10mg-200mg Tablet(Ibuprofen)
Tobacco and Nonsteroidal antiinflammatory drugs (systemic)(Ibuprofen)
Side effects from Nonsteroidal anti-inflammatory drugs may get worse if you use tobacco-containing products such as cigarettes. If you have persistent stomach upset, vomit blood or what looks like coffee grounds, or have black, tarry stools, contact your health care provider immediately. Many non-prescription products contain NSAIDs; closely read labels before taking any medicines. Eye or Skin products containing NSAIDs should not interact with tobacco.
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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