Product NDC: | 50242-100 |
Proprietary Name: | Pulmozyme |
Non Proprietary Name: | dornase alfa |
Active Ingredient(s): | 1 mg/mL & nbsp; dornase alfa |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50242-100 |
Labeler Name: | Genentech, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA103532 |
Marketing Category: | BLA |
Start Marketing Date: | 19931230 |
Package NDC: | 50242-100-40 |
Package Description: | 5 POUCH in 1 CARTON (50242-100-40) > 6 AMPULE in 1 POUCH > 2.5 mL in 1 AMPULE |
NDC Code | 50242-100-40 |
Proprietary Name | Pulmozyme |
Package Description | 5 POUCH in 1 CARTON (50242-100-40) > 6 AMPULE in 1 POUCH > 2.5 mL in 1 AMPULE |
Product NDC | 50242-100 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | dornase alfa |
Dosage Form Name | SOLUTION |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 19931230 |
Marketing Category Name | BLA |
Labeler Name | Genentech, Inc. |
Substance Name | DORNASE ALFA |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Decreased Respiratory Secretion Viscosity [PE],Deoxyribonuclease I [Chemical/Ingredient],Recombinant Human Deoxyribonuclease 1 [EPC],Recombinant Proteins [Chemical/Ingredient] |