Drug application
GENTAK (GENTAMICIN SULFATE)
Drugs@FDA ANDA 064163 · PHARMOBEDIENT
Key facts
| Drug name | GENTAK |
|---|---|
| Active ingredients | GENTAMICIN SULFATE |
| Application type | ANDA |
| Application number | 064163 |
| Company | PHARMOBEDIENT |
| Dosage forms | SOLUTION/DROPS, OPHTHALMIC |
| Strength | EQ 0.3% BASE |
| Marketing status | Discontinued |
| TE codes | AT |
| Reference listed drug | No |
| Latest submission status date | Oct 12, 2001 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- 1–9 Therapeutic equivalents
- Yes FDA letters on file
- No 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: