ZERIT - 0003-1967-01 - (stavudine)

Alphabetical Index


Drug Information of ZERIT

Product NDC: 0003-1967
Proprietary Name: ZERIT
Non Proprietary Name: stavudine
Active Ingredient(s): 40    mg/1 & nbsp;   stavudine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ZERIT

Product NDC: 0003-1967
Labeler Name: E.R. Squibb & Sons, L.L.C.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020412
Marketing Category: NDA
Start Marketing Date: 19940624

Package Information of ZERIT

Package NDC: 0003-1967-01
Package Description: 60 CAPSULE, GELATIN COATED in 1 BOTTLE (0003-1967-01)

NDC Information of ZERIT

NDC Code 0003-1967-01
Proprietary Name ZERIT
Package Description 60 CAPSULE, GELATIN COATED in 1 BOTTLE (0003-1967-01)
Product NDC 0003-1967
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name stavudine
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 19940624
Marketing Category Name NDA
Labeler Name E.R. Squibb & Sons, L.L.C.
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 ZERIT


General Information