Home
>
National Drug Code (NDC)
>
FUZEON
FUZEON - 0004-0381-40 - (Enfuvirtide)
Drug Information of FUZEON
| Product NDC: | 0004-0381 |
| Proprietary Name: | FUZEON |
| Non Proprietary Name: | Enfuvirtide |
| Active Ingredient(s): | & nbsp; Enfuvirtide |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FUZEON
| Product NDC: | 0004-0381 |
| Labeler Name: | Genentech, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021481 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120410 |
Package Information of FUZEON
| Package NDC: | 0004-0381-40 |
| Package Description: | 1 KIT in 1 CARTON (0004-0381-40) * 1 mL in 1 VIAL, SINGLE-USE * 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of FUZEON
| NDC Code | 0004-0381-40 |
| Proprietary Name | FUZEON |
| Package Description | 1 KIT in 1 CARTON (0004-0381-40) * 1 mL in 1 VIAL, SINGLE-USE * 1 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0004-0381 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Enfuvirtide |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20120410 |
| Marketing Category Name | NDA |
| Labeler Name | Genentech, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
