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Pentostatin
Pentostatin - 55390-244-01 - (Pentostatin)
Drug Information of Pentostatin
| Product NDC: | 55390-244 |
| Proprietary Name: | Pentostatin |
| Non Proprietary Name: | Pentostatin |
| Active Ingredient(s): | 10 mg/5mL & nbsp; Pentostatin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pentostatin
| Product NDC: | 55390-244 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077841 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070813 |
Package Information of Pentostatin
| Package NDC: | 55390-244-01 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 BOX (55390-244-01) > 5 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Pentostatin
| NDC Code | 55390-244-01 |
| Proprietary Name | Pentostatin |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 BOX (55390-244-01) > 5 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 55390-244 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pentostatin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20070813 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | PENTOSTATIN |
| Strength Number | 10 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
