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Sulfasalazine - 59762-0104-1 - (SULFASALAZINE)

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Drug Information of Sulfasalazine

Product NDC: 59762-0104
Proprietary Name: Sulfasalazine
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 Sulfasalazine

Product NDC: 59762-0104
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA007073
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20050505

Package Information of Sulfasalazine

Package NDC: 59762-0104-1
Package Description: 100 TABLET, DELAYED RELEASE in 1 BOTTLE (59762-0104-1)

NDC Information of Sulfasalazine

NDC Code 59762-0104-1
Proprietary Name Sulfasalazine
Package Description 100 TABLET, DELAYED RELEASE in 1 BOTTLE (59762-0104-1)
Product NDC 59762-0104
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SULFASALAZINE
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20050505
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name SULFASALAZINE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Aminosalicylate [EPC],Aminosalicylic Acids [Chemical/Ingredient]

Complete Information of Sulfasalazine


General Information