| NDC Code | 0013-8727-89 |
|---|
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (0013-8727-89) > 50 mL in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 0013-8727 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Zinecard |
|---|
| Non-Proprietary Name | Dexrazoxane |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 19950526 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA020212 |
|---|
| Manufacturer | Pharmacia and Upjohn Company LLC |
|---|
| Substance Name | DEXRAZOXANE HYDROCHLORIDE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/50mL |
|---|
| Pharmacy Classes | Cytoprotective Agent [EPC] |
|---|