Oxaliplatin - Oxaliplatin
Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE| Field | Value |
|---|---|
| NDC Code: | 47335-178 |
| Proprietary Name: | Oxaliplatin |
| Suffix: | |
| Non-Proprietary Name: | Oxaliplatin |
| Dosage Form: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Method: | INTRAVENOUS |
| Original Marketing Date: | 19-08-2009 |
| Category Name: | ANDA |
| Application Number: | ANDA078818 |
| Labeler: | SUN PHARMA GLOBAL FZE |
| Substance Name: | OXALIPLATIN |
| Active Numerator Strength: | 100 |
| Active Ingredient Unit: | mg/20mL |
| Pharm Classes: | Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient] |
| DEA Schedule: |