GEMCITABINE HYDROCHLORIDE (GEMCITABINE HYDROCHLORIDE) — FDA Approval ANDA213175 (HIKMA)
GEMCITABINE HYDROCHLORIDE (GEMCITABINE HYDROCHLORIDE) — FDA Approval ANDA213175 (HIKMA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: GEMCITABINE HYDROCHLORIDE; Active ingredients: GEMCITABINE HYDROCHLORIDE; Application number: ANDA213175.
| Brand name | GEMCITABINE HYDROCHLORIDE |
|---|---|
| Active ingredients | GEMCITABINE HYDROCHLORIDE |
| Application number | ANDA213175 |
| Sponsor | HIKMA |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Marketing status | Prescription |
| Products in application | 3 |
| First approval date | 20230307 |
| Source | openFDA Drugs@FDA |
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