Drug application
GEMCITABINE HYDROCHLORIDE (GEMCITABINE HYDROCHLORIDE)
Drugs@FDA ANDA 202063 · EMCURE PHARMS LTD
Key facts
| Drug name | GEMCITABINE HYDROCHLORIDE |
|---|---|
| Active ingredients | GEMCITABINE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 202063 |
| Company | EMCURE PHARMS LTD |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | EQ 200MG BASE/VIAL |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission class | Not Applicable |
| Latest submission status date | Sep 11, 2012 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
- No FDA letters on file
- Yes FDA reviews on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: