Stavudine - 53808-0594-1 - (Stavudine)

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Drug Information of Stavudine

Product NDC: 53808-0594
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: 53808-0594
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079069
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Stavudine

Package NDC: 53808-0594-1
Package Description: 30 CAPSULE in 1 BLISTER PACK (53808-0594-1)

NDC Information of Stavudine

NDC Code 53808-0594-1
Proprietary Name Stavudine
Package Description 30 CAPSULE in 1 BLISTER PACK (53808-0594-1)
Product NDC 53808-0594
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Stavudine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
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


General Information