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Cytarabine
Cytarabine - 0069-0153-02 - (Cytarabine)
Drug Information of Cytarabine
| Product NDC: | 0069-0153 |
| Proprietary Name: | Cytarabine |
| Non Proprietary Name: | Cytarabine |
| Active Ingredient(s): | 20 mg/mL & nbsp; Cytarabine |
| Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cytarabine
| Product NDC: | 0069-0153 |
| Labeler Name: | Pfizer Laboratories Div Pfizer Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200916 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111214 |
Package Information of Cytarabine
| Package NDC: | 0069-0153-02 |
| Package Description: | 10 VIAL in 1 CARTON (0069-0153-02) > 25 mL in 1 VIAL (0069-0153-01) |
NDC Information of Cytarabine
| NDC Code | 0069-0153-02 |
| Proprietary Name | Cytarabine |
| Package Description | 10 VIAL in 1 CARTON (0069-0153-02) > 25 mL in 1 VIAL (0069-0153-01) |
| Product NDC | 0069-0153 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cytarabine |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20111214 |
| Marketing Category Name | ANDA |
| Labeler Name | Pfizer Laboratories Div Pfizer Inc. |
| Substance Name | CYTARABINE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
