Azulfidine EN-tabs 500 mg/1
Sulfasalazine · TABLET, DELAYED RELEASE · Pfizer Laboratories Div Pfizer Inc
Azulfidine EN-tabs is a tablet, delayed release containing sulfasalazine at 500 mg/1, taken oral. Manufactured by Pfizer Laboratories Div Pfizer Inc.
Key Facts
- Brand Name
- Azulfidine EN-tabs
- Generic Name
- Sulfasalazine
- NDC Code (Product)
0013-0102- Manufacturer
- Pfizer Laboratories Div Pfizer Inc
- Strength
- 500 mg/1
- Dosage Form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- NDA007073
- Drug Class
- Aminosalicylate [EPC]
- Marketing Start
- 06/20/1950
Recall History
No Recall HistoryFrequently Asked Questions
What is Azulfidine EN-tabs used for?
Azulfidine EN-tabs contains Sulfasalazine. It is a tablet, delayed release taken oral. Consult your doctor for specific uses.
Is Azulfidine EN-tabs a controlled substance?
Azulfidine EN-tabs is not classified as a controlled substance by the DEA.
What is the generic name for Azulfidine EN-tabs?
The generic name for Azulfidine EN-tabs is Sulfasalazine. There are 11 other brand versions of Sulfasalazine.
What is the NDC code for Azulfidine EN-tabs 500 mg/1?
The NDC (National Drug Code) for Azulfidine EN-tabs 500 mg/1 is 0013-0102, listed by Pfizer Laboratories Div Pfizer Inc.
Other Sulfasalazine Brands
See all →- Sulfasalazine500 mg/171610-706
- Sulfasalazine500 mg/111534-200
- Sulfasalazine500 mg/111534-201
- Sulfasalazine500 mg/150090-6936
- Sulfasalazine500 mg/170518-1829
- Sulfasalazine500 mg/116571-261
- Sulfasalazine500 mg/10093-3234
- Sulfasalazine500 mg/159762-0104
- Sulfasalazine500 mg/163629-9715
- Sulfasalazine500 mg/150090-0086
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
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