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SULFASALAZINE - 54868-1138-7 - (Sulfasalazine)

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Drug Information of SULFASALAZINE

Product NDC: 54868-1138
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: 54868-1138
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021243
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20021206

Package Information of SULFASALAZINE

Package NDC: 54868-1138-7
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (54868-1138-7)

NDC Information of SULFASALAZINE

NDC Code 54868-1138-7
Proprietary Name SULFASALAZINE
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (54868-1138-7)
Product NDC 54868-1138
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulfasalazine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20021206
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, 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