Home > National Drug Code (NDC) > Sulfasalazine

Sulfasalazine - 0904-1152-40 - (Sulfasalazine)

Alphabetical Index


Drug Information of Sulfasalazine

Product NDC: 0904-1152
Proprietary Name: Sulfasalazine
Non Proprietary Name: Sulfasalazine
Active Ingredient(s): 500    mg/1 & nbsp;   Sulfasalazine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sulfasalazine

Product NDC: 0904-1152
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021243
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20000818

Package Information of Sulfasalazine

Package NDC: 0904-1152-40
Package Description: 500 TABLET in 1 BOTTLE (0904-1152-40)

NDC Information of Sulfasalazine

NDC Code 0904-1152-40
Proprietary Name Sulfasalazine
Package Description 500 TABLET in 1 BOTTLE (0904-1152-40)
Product NDC 0904-1152
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulfasalazine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000818
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Major Pharmaceuticals
Substance Name SULFASALAZINE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Aminosalicylate [EPC],Aminosalicylic Acids [Chemical/Ingredient]

Complete Information of Sulfasalazine


General Information