Cytarabine is a Intrathecal; Intravenous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Fresenius Kabi Usa, Llc. The primary component is Cytarabine.
Product ID | 63323-120_6594799a-7b02-4847-aff7-1cb7842771bd |
NDC | 63323-120 |
Product Type | Human Prescription Drug |
Proprietary Name | Cytarabine |
Generic Name | Cytarabine |
Dosage Form | Injection, Solution |
Route of Administration | INTRATHECAL; INTRAVENOUS; SUBCUTANEOUS |
Marketing Start Date | 2004-11-29 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA076512 |
Labeler Name | Fresenius Kabi USA, LLC |
Substance Name | CYTARABINE |
Active Ingredient Strength | 100 mg/mL |
Pharm Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2004-11-29 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA076512 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2004-11-29 |
Ingredient | Strength |
---|---|
CYTARABINE | 100 mg/mL |
SPL SET ID: | c4fdc56e-efd7-4825-a518-ef430b2b3df0 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
61703-303 | CYTARABINE | CYTARABINE |
61703-304 | Cytarabine | CYTARABINE |
61703-305 | Cytarabine | CYTARABINE |
61703-319 | Cytarabine | CYTARABINE |
63323-120 | Cytarabine | CYTARABINE |
67457-452 | Cytarabine | Cytarabine |
67457-454 | Cytarabine | Cytarabine |
67457-455 | cytarabine | cytarabine |
68083-337 | Cytarabine | Cytarabine |
68083-343 | Cytarabine | Cytarabine |
71288-108 | Cytarabine | Cytarabine |
71288-109 | Cytarabine | Cytarabine |
71288-168 | Cytarabine | Cytarabine |
71288-169 | Cytarabine | Cytarabine |