NDC 69097-514
Abacavir
Abacavir
Abacavir is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Cipla Usa Inc.. The primary component is Abacavir Sulfate.
| Product ID | 69097-514_111c0e04-abba-40e6-ab23-2df93e429250 |
| NDC | 69097-514 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Abacavir |
| Generic Name | Abacavir |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2017-11-21 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA078119 |
| Labeler Name | Cipla USA Inc. |
| Substance Name | ABACAVIR SULFATE |
| Active Ingredient Strength | 300 mg/1 |
| Pharm Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |