Gemcitabine Hydrochloride - Gemcitabine Hydrochloride
Navigation: NDC > Supplier starting with: T > TEVA PARENTERAL MEDICINES, INC.| Field | Value |
|---|---|
| NDC Code: | 0703-5775 |
| Proprietary Name: | Gemcitabine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Gemcitabine Hydrochloride |
| Dosage Form: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Method: | INTRAVENOUS |
| Original Marketing Date: | 14-07-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA077983 |
| Labeler: | TEVA PARENTERAL MEDICINES, INC. |
| Substance Name: | GEMCITABINE HYDROCHLORIDE |
| Active Numerator Strength: | 200 |
| Active Ingredient Unit: | mg/5mL |
| Pharm Classes: | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
| DEA Schedule: |