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Sulfadiazine - 0185-0757-30 - (Sulfadiazine)

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Drug Information of Sulfadiazine

Product NDC: 0185-0757
Proprietary Name: Sulfadiazine
Non Proprietary Name: Sulfadiazine
Active Ingredient(s): 500    mg/1 & nbsp;   Sulfadiazine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sulfadiazine

Product NDC: 0185-0757
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040091
Marketing Category: ANDA
Start Marketing Date: 19940729

Package Information of Sulfadiazine

Package NDC: 0185-0757-30
Package Description: 30 TABLET in 1 BOTTLE (0185-0757-30)

NDC Information of Sulfadiazine

NDC Code 0185-0757-30
Proprietary Name Sulfadiazine
Package Description 30 TABLET in 1 BOTTLE (0185-0757-30)
Product NDC 0185-0757
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulfadiazine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19940729
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name SULFADIAZINE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Sulfadiazine


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