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oxaliplatin
oxaliplatin - 63323-650-17 - (oxaliplatin)
Drug Information of oxaliplatin
| Product NDC: | 63323-650 |
| Proprietary Name: | oxaliplatin |
| Non Proprietary Name: | oxaliplatin |
| Active Ingredient(s): | 5 mg/mL & nbsp; oxaliplatin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of oxaliplatin
| Product NDC: | 63323-650 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078811 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100611 |
Package Information of oxaliplatin
| Package NDC: | 63323-650-17 |
| Package Description: | 10 BOX in 1 CARTON (63323-650-17) > 1 VIAL in 1 BOX > 10 mL in 1 VIAL |
NDC Information of oxaliplatin
| NDC Code | 63323-650-17 |
| Proprietary Name | oxaliplatin |
| Package Description | 10 BOX in 1 CARTON (63323-650-17) > 1 VIAL in 1 BOX > 10 mL in 1 VIAL |
| Product NDC | 63323-650 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxaliplatin |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100611 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | OXALIPLATIN |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient] |
