| Product NDC: | 0085-1368 |
| Proprietary Name: | PEGINTRON |
| Non Proprietary Name: | peginterferon alfa-2b |
| Active Ingredient(s): | & nbsp; peginterferon alfa-2b |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0085-1368 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103949 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20010119 |
| Package NDC: | 0085-1368-01 |
| Package Description: | 1 KIT in 1 CARTON (0085-1368-01) * .5 mL in 1 VIAL * 1.25 mL in 1 VIAL |
| NDC Code | 0085-1368-01 |
| Proprietary Name | PEGINTRON |
| Package Description | 1 KIT in 1 CARTON (0085-1368-01) * .5 mL in 1 VIAL * 1.25 mL in 1 VIAL |
| Product NDC | 0085-1368 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | peginterferon alfa-2b |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20010119 |
| Marketing Category Name | BLA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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