Product NDC: | 55390-337 |
Proprietary Name: | Dactinomycin |
Non Proprietary Name: | Dactinomycin |
Active Ingredient(s): | 500 ug/1 & nbsp; Dactinomycin |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55390-337 |
Labeler Name: | Bedford Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090304 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100712 |
Package NDC: | 55390-337-01 |
Package Description: | 1 VIAL in 1 BOX (55390-337-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
NDC Code | 55390-337-01 |
Proprietary Name | Dactinomycin |
Package Description | 1 VIAL in 1 BOX (55390-337-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
Product NDC | 55390-337 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dactinomycin |
Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100712 |
Marketing Category Name | ANDA |
Labeler Name | Bedford Laboratories |
Substance Name | DACTINOMYCIN |
Strength Number | 500 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Actinomycin [EPC],Nucleic Acid Synthesis Inhibitors [MoA],Protein Synthesis Inhibitors [MoA] |