| 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] |