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ZIAGEN
ZIAGEN - 53808-0811-1 - (abacavir sulfate)
Drug Information of ZIAGEN
| Product NDC: | 53808-0811 |
| Proprietary Name: | ZIAGEN |
| Non Proprietary Name: | abacavir sulfate |
| Active Ingredient(s): | 300 mg/1 & nbsp; abacavir sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZIAGEN
| Product NDC: | 53808-0811 |
| Labeler Name: | State of Florida DOH Central Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020977 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090701 |
Package Information of ZIAGEN
| Package NDC: | 53808-0811-1 |
| Package Description: | 1 TABLET, FILM COATED in 1 BLISTER PACK (53808-0811-1) |
NDC Information of ZIAGEN
| NDC Code | 53808-0811-1 |
| Proprietary Name | ZIAGEN |
| Package Description | 1 TABLET, FILM COATED in 1 BLISTER PACK (53808-0811-1) |
| Product NDC | 53808-0811 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | abacavir sulfate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | NDA |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | ABACAVIR SULFATE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
