| NDC Code | 0002-7501-01 |
|---|
| Package Description | 5 mL in 1 VIAL, SINGLE-DOSE (0002-7501-01) |
|---|
| Product NDC | 0002-7501 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Gemzar |
|---|
| Non-Proprietary Name | Gemcitabine Hydrochloride |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 19960515 |
|---|
| End Marketing Date | 20210531 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA020509 |
|---|
| Manufacturer | Eli Lilly and Company |
|---|
| Substance Name | GEMCITABINE HYDROCHLORIDE |
|---|
| Strength | 200 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
|---|