| NDC Code | 0703-5775-01 |
|---|
| Package Description | 1 VIAL in 1 CARTON (0703-5775-01) > 5 mL in 1 VIAL |
|---|
| Product NDC | 0703-5775 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Gemcitabine Hydrochloride |
|---|
| Non-Proprietary Name | Gemcitabine Hydrochloride |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20110714 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077983 |
|---|
| Manufacturer | Teva Parenteral Medicines, Inc. |
|---|
| Substance Name | GEMCITABINE HYDROCHLORIDE |
|---|
| Strength | 200 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
|---|