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SULFASALAZINE - 68788-9021-3 - (SULFASALAZINE)

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Drug Information of SULFASALAZINE

Product NDC: 68788-9021
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: 68788-9021
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087197
Marketing Category: ANDA
Start Marketing Date: 20100609

Package Information of SULFASALAZINE

Package NDC: 68788-9021-3
Package Description: 30 TABLET in 1 BOTTLE, DISPENSING (68788-9021-3)

NDC Information of SULFASALAZINE

NDC Code 68788-9021-3
Proprietary Name SULFASALAZINE
Package Description 30 TABLET in 1 BOTTLE, DISPENSING (68788-9021-3)
Product NDC 68788-9021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SULFASALAZINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100609
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name SULFASALAZINE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Aminosalicylate [EPC],Aminosalicylic Acids [Chemical/Ingredient]

Complete Information of SULFASALAZINE


General Information