Product NDC: | 0085-1312 |
Proprietary Name: | SYLATRON |
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: | 0085-1312 |
Labeler Name: | Merck Sharp & Dohme Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA103949 |
Marketing Category: | BLA |
Start Marketing Date: | 20110329 |
Package NDC: | 0085-1312-01 |
Package Description: | 1 KIT in 1 CARTON (0085-1312-01) * .1 mL in 1 VIAL * 1.25 mL in 1 VIAL (0085-0061-02) |
NDC Code | 0085-1312-01 |
Proprietary Name | SYLATRON |
Package Description | 1 KIT in 1 CARTON (0085-1312-01) * .1 mL in 1 VIAL * 1.25 mL in 1 VIAL (0085-0061-02) |
Product NDC | 0085-1312 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | peginterferon alfa-2b |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20110329 |
Marketing Category Name | BLA |
Labeler Name | Merck Sharp & Dohme Corp. |
Substance Name | |
Strength Number | |
Strength Unit | |
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