Home
>
National Drug Code (NDC)
>
ACTIMMUNE
ACTIMMUNE - 64116-011-12 - (Interferon gamma-1b)
Drug Information of ACTIMMUNE
| Product NDC: | 64116-011 |
| Proprietary Name: | ACTIMMUNE |
| Non Proprietary Name: | Interferon gamma-1b |
| Active Ingredient(s): | 100 ug/.5mL & nbsp; Interferon gamma-1b |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ACTIMMUNE
| Product NDC: | 64116-011 |
| Labeler Name: | InterMune, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103836 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19990225 |
Package Information of ACTIMMUNE
| Package NDC: | 64116-011-12 |
| Package Description: | 12 VIAL, SINGLE-USE in 1 CARTON (64116-011-12) > .5 mL in 1 VIAL, SINGLE-USE (64116-011-01) |
NDC Information of ACTIMMUNE
| NDC Code | 64116-011-12 |
| Proprietary Name | ACTIMMUNE |
| Package Description | 12 VIAL, SINGLE-USE in 1 CARTON (64116-011-12) > .5 mL in 1 VIAL, SINGLE-USE (64116-011-01) |
| Product NDC | 64116-011 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Interferon gamma-1b |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 19990225 |
| Marketing Category Name | BLA |
| Labeler Name | InterMune, Inc. |
| Substance Name | INTERFERON GAMMA-1B |
| Strength Number | 100 |
| Strength Unit | ug/.5mL |
| Pharmaceutical Classes | Interferon gamma [EPC],Interferon-gamma [Chemical/Ingredient] |
