Sovaldi is a Oral Pellet in the Human Prescription Drug category. It is labeled and distributed by Gilead Sciences, Inc.. The primary component is Sofosbuvir.
| Product ID | 61958-1505_10e67d0d-c67d-4971-a948-b733c476e603 |
| NDC | 61958-1505 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Sovaldi |
| Generic Name | Sofosbuvir |
| Dosage Form | Pellet |
| Route of Administration | ORAL |
| Marketing Start Date | 2019-08-28 |
| Marketing Category | NDA / NDA |
| Application Number | NDA212480 |
| Labeler Name | Gilead Sciences, Inc. |
| Substance Name | SOFOSBUVIR |
| Active Ingredient Strength | 200 mg/1 |
| Pharm Classes | Hepatitis C Virus Nucleotide Analog NS5B Polymerase Inhibitor [EPC],RNA Replicase Inhibitors [MoA],Nucleoside Analog [EXT] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2019-08-28 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA212480 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-08-28 |
| Ingredient | Strength |
|---|---|
| SOFOSBUVIR | 200 mg/1 |
| SPL SET ID: | 80beab2c-396e-4a37-a4dc-40fdb62859cf |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 61958-1501 | Sovaldi | SOFOSBUVIR |
| 61958-1503 | Sovaldi | SOFOSBUVIR |
| 61958-1504 | Sovaldi | SOFOSBUVIR |
| 61958-1505 | Sovaldi | SOFOSBUVIR |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SOVALDI 85709308 4468665 Live/Registered |
GILEAD SCIENCES IRELAND UC 2012-08-21 |