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Oxaliplatin
Oxaliplatin - 47335-178-40 - (Oxaliplatin)
Drug Information of Oxaliplatin
| Product NDC: | 47335-178 |
| Proprietary Name: | Oxaliplatin |
| Non Proprietary Name: | Oxaliplatin |
| Active Ingredient(s): | 100 mg/20mL & nbsp; Oxaliplatin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxaliplatin
| Product NDC: | 47335-178 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078818 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090819 |
Package Information of Oxaliplatin
| Package NDC: | 47335-178-40 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (47335-178-40) > 20 mL in 1 VIAL, SINGLE-USE |
NDC Information of Oxaliplatin
| NDC Code | 47335-178-40 |
| Proprietary Name | Oxaliplatin |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (47335-178-40) > 20 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 47335-178 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxaliplatin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090819 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | OXALIPLATIN |
| Strength Number | 100 |
| Strength Unit | mg/20mL |
| Pharmaceutical Classes | Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient] |
