Azulfidine Oral Tablet 500Mg Drug Medication Dosage Information
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Azulfidine: Oral tablet (500mg)

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Drug Image file DrugItem_4041.JPG
Sulfasalazine 500mg Tab
Major Pharmaceuticals Inc
Pill Identification: MP 91 
Drug Image file DrugItem_9464.JPG
Sulfasalazine 500mg Tab
Major Pharmaceuticals Inc
Pill Identification: MP 91 
Drug Image file DrugItem_4040.JPG
Sulfasalazine 500mg Tab
Sun Pharmaceutical Industries, Inc.
Pill Identification: MP 91 
Drug Image file DrugItem_771.JPG
Azulfidine 500mg Tab
Pfizer US Pharmaceuticals
Pill Identification: KPh  |  101
Drug Image file DrugItem_1649.JPG
Sulfasalazine 500mg Tab
Greenstone Ltd
Pill Identification: G 500 
Drug Image file DrugItem_16565.JPG
Sulfazine 500mg Tab
Qualitest Pharmaceuticals Inc
Pill Identification: 5904 V 
Drug Image file DrugItem_384.JPG
Sulfasalazine 500mg Tab
Actavis Inc. formerly Watson Pharmaceuticals Inc
Pill Identification: WATSON 796 
Drug Image file DrugItem_17719.JPG
Sulfasalazine 500mg Tab
AvPAK; a Division of AvKARE Inc
Pill Identification: WATSON 796 
Drug Image file DrugItem_2996.JPG
Sulfasalazine 500mg Tab
United Research Laboratories, Inc. a subsidiary of Sun Pharmaceutical Industries, Inc.
Pill Identification: MP 91 

What is this Medicine?

SULFASALAZINE (sul fa SAL a zeen) is used to treat ulcerative colitis.

Similar Generic Drugs : Sulfasalazine: Oral tablet (500mg)
In-Depth Information

Azulfidine 500mg Tablet

NDC: 000130101
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Rheumatoid Arthritis, Ulcerative Colitis

Sometimes used for but not FDA approved for the following conditions:
Crohn's Disease

Storage Information
Store at 77 degrees F; excursions permitted to 59-86 degrees F
Azulfidine 500mg Tablet
Drug Image file DrugItem_771.JPG
Pfizer US Pharmaceuticals
Pill Identification: KPh  |  101
Shape: round
Color: orange

Reported Side Effects for Azulfidine 500mg Tablet

Hives Incidence:
<3.3%*
Severity: MILD
Onset: RAPID
Skin Rash Incidence:
<13.0%*
Severity: MILD
Onset: EARLY
Diuresis Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Cyanosis Incidence:
<3.3%*
Severity: SEVERE
Onset: EARLY
Low Blood Sugar Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Hemolytic Anemia Incidence:
<3.3%*
Severity: SEVERE
Onset: DELAYED
Enlarged Thyroid Gland Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Fever Incidence:
<5.0%*
Severity: MILD
Onset: EARLY
Itching Incidence:
<4.0%*
Severity: MILD
Onset: RAPID
Low Platelet Count Incidence:
1.0%*
Severity: MODERATE
Onset: DELAYED
Low White Blood Cell Counts Incidence:
3.0%*
Severity: MODERATE
Onset: DELAYED
Elevated Hepatic Enzymes Incidence:
4.0%*
Severity: MODERATE
Onset: DELAYED
Lightheadedness Incidence:
4.0%*
Severity: MILD
Onset: EARLY
Mouth Ulcers Incidence:
4.0%*
Severity: MODERATE
Onset: DELAYED
Stomach Pain Incidence:
8.0%*
Severity: MILD
Onset: EARLY
Vomiting Incidence:
8.0-33.0%*
Severity: MILD
Onset: EARLY
Headache Incidence:
9.0-33.0%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
13.0%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
19.0-33.0%*
Severity: MILD
Onset: EARLY
Low Sperm Count Incidence:
33.0%*
Severity: MILD
Onset: DELAYED
Decreased Appetite Incidence:
33.0%*
Severity: MILD
Onset: DELAYED
*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.
Pregnancy & Lactation Information
FIRST Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

SECOND Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

THIRD Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

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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