0013-0102 : Azulfidine 500 mg Enteric Coated Tablet


NDC0013-0102
Labeler: Pharmacia and Upjohn Company
Product Type: Human Prescription Drug
Drug Name:  Azulfidine En-tabs
Dosage Form: Oral Tablet, Delayed Release
Application #: NDA007073
Rev. Date: 


Appearance:


Markings: 102;KPh
Shapes:  Oval
Colors:  Yellow
Size (mm): 18
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

102 KPh: (0013-0102) Azulfidine 500 mg Enteric Coated Tablet by Pharmacia and Upjohn Company
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 0013-0102-01: 100 TABLET, DELAYED RELEASE IN 1 BOTTLE (0013‑0102‑01)
  • 0013-0102-20: 300 TABLET, DELAYED RELEASE IN 1 BOTTLE (0013‑0102‑20)

Active Ingredients:

  • Sulfasalazine

Dosage Strength:

  • 500 mg

Inactive Ingredients:

  • Cellulose Acetate
  • Povidones
  • Magnesium Stearate
  • Silicon Dioxide
  • Propylene Glycol
  • Talc
  • Carnauba Wax
  • Glyceryl Monostearate
  • White Wax
  • Acetone
  • Alcohol

Pharmaceutical Classes:

  • Aminosalicylate [EPC]
  • Aminosalicylic Acids [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 0013-0101 Azulfidine 500 mg Oral Tablet by Pharmacia and Upjohn Company

NDC QR Code

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NDC 0013-0102 QR Code

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