Stavudine - 31722-518-05 - (Stavudine)

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Drug Information of Stavudine

Product NDC: 31722-518
Proprietary Name: Stavudine
Non Proprietary Name: Stavudine
Active Ingredient(s): 40    mg/1 & nbsp;   Stavudine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Stavudine

Product NDC: 31722-518
Labeler Name: Camber Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078957
Marketing Category: ANDA
Start Marketing Date: 20081229

Package Information of Stavudine

Package NDC: 31722-518-05
Package Description: 500 CAPSULE in 1 BOTTLE (31722-518-05)

NDC Information of Stavudine

NDC Code 31722-518-05
Proprietary Name Stavudine
Package Description 500 CAPSULE in 1 BOTTLE (31722-518-05)
Product NDC 31722-518
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Stavudine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20081229
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals, Inc.
Substance Name STAVUDINE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

Complete Information of Stavudine


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