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SULFASALAZINE - 49349-067-02 - (SULFASALAZINE)

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Drug Information of SULFASALAZINE

Product NDC: 49349-067
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: 49349-067
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085828
Marketing Category: ANDA
Start Marketing Date: 20101115

Package Information of SULFASALAZINE

Package NDC: 49349-067-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-067-02)

NDC Information of SULFASALAZINE

NDC Code 49349-067-02
Proprietary Name SULFASALAZINE
Package Description 30 TABLET in 1 BLISTER PACK (49349-067-02)
Product NDC 49349-067
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SULFASALAZINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101115
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name SULFASALAZINE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Aminosalicylate [EPC],Aminosalicylic Acids [Chemical/Ingredient]

Complete Information of SULFASALAZINE


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