NDC 70518-0559
Abacavir
Abacavir
Abacavir is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Abacavir Sulfat.
| Product ID | 70518-0559_50ebc53e-1458-34d2-e054-00144ff88e88 |
| NDC | 70518-0559 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Abacavir |
| Generic Name | Abacavir |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2017-05-30 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA077844 |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | ABACAVIR SULFAT |
| Active Ingredient Strength | 300 mg/1 |
| Pharm Classes | Human Immunodef |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |