ZIAGEN - 49702-222-48 - (abacavir sulfate)

Alphabetical Index


Drug Information of ZIAGEN

Product NDC: 49702-222
Proprietary Name: ZIAGEN
Non Proprietary Name: abacavir sulfate
Active Ingredient(s): 20    mg/mL & nbsp;   abacavir sulfate
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ZIAGEN

Product NDC: 49702-222
Labeler Name: ViiV Healthcare Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020978
Marketing Category: NDA
Start Marketing Date: 19990128

Package Information of ZIAGEN

Package NDC: 49702-222-48
Package Description: 240 mL in 1 BOTTLE (49702-222-48)

NDC Information of ZIAGEN

NDC Code 49702-222-48
Proprietary Name ZIAGEN
Package Description 240 mL in 1 BOTTLE (49702-222-48)
Product NDC 49702-222
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name abacavir sulfate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19990128
Marketing Category Name NDA
Labeler Name ViiV Healthcare Company
Substance Name ABACAVIR SULFATE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

Complete Information of ZIAGEN


General Information