| Product NDC: | 0004-0350 |
| Proprietary Name: | Pegasys |
| Non Proprietary Name: | peginterferon alfa-2a |
| Active Ingredient(s): | 180 ug/mL & nbsp; peginterferon alfa-2a |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0004-0350 |
| Labeler Name: | Genentech, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103964 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20021016 |
| Package NDC: | 0004-0350-09 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 BOX (0004-0350-09) > 1 mL in 1 VIAL, SINGLE-USE |
| NDC Code | 0004-0350-09 |
| Proprietary Name | Pegasys |
| Package Description | 1 VIAL, SINGLE-USE in 1 BOX (0004-0350-09) > 1 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0004-0350 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | peginterferon alfa-2a |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20021016 |
| Marketing Category Name | BLA |
| Labeler Name | Genentech, Inc. |
| Substance Name | PEGINTERFERON ALFA-2A |
| Strength Number | 180 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Interferon alpha [EPC],peginterferon alfa-2a [Chemical/Ingredient] |