Azulfidine - 0013-0102-01 - (SULFASALAZINE)

Alphabetical Index


Drug Information of Azulfidine

Product NDC: 0013-0102
Proprietary Name: Azulfidine
Non Proprietary Name: SULFASALAZINE
Active Ingredient(s): 500    mg/1 & nbsp;   SULFASALAZINE
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Azulfidine

Product NDC: 0013-0102
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA007073
Marketing Category: NDA
Start Marketing Date: 19500620

Package Information of Azulfidine

Package NDC: 0013-0102-01
Package Description: 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0013-0102-01)

NDC Information of Azulfidine

NDC Code 0013-0102-01
Proprietary Name Azulfidine
Package Description 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0013-0102-01)
Product NDC 0013-0102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SULFASALAZINE
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 19500620
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name SULFASALAZINE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Aminosalicylate [EPC],Aminosalicylic Acids [Chemical/Ingredient]

Complete Information of Azulfidine


General Information