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Abacavir Sulfate
Abacavir Sulfate - 51079-204-06 - (abacavir sulfate)
Drug Information of Abacavir Sulfate
| Product NDC: | 51079-204 |
| Proprietary Name: | Abacavir Sulfate |
| 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 Abacavir Sulfate
| Product NDC: | 51079-204 |
| Labeler Name: | Mylan Institutional Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091294 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130218 |
Package Information of Abacavir Sulfate
| Package NDC: | 51079-204-06 |
| Package Description: | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-204-06) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-204-01) |
NDC Information of Abacavir Sulfate
| NDC Code | 51079-204-06 |
| Proprietary Name | Abacavir Sulfate |
| Package Description | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-204-06) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-204-01) |
| Product NDC | 51079-204 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | abacavir sulfate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130218 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional Inc. |
| 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] |
