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