Drug application
SODIUM PHENYLACETATE AND SODIUM BENZOATE (SODIUM BENZOATE, SODIUM PHENYLACETATE)
Drugs@FDA ANDA 208521 · MAIA PHARMS INC
Key facts
| Drug name | SODIUM PHENYLACETATE AND SODIUM BENZOATE |
|---|---|
| Active ingredients | SODIUM BENZOATE, SODIUM PHENYLACETATE |
| Application type | ANDA |
| Application number | 208521 |
| Company | MAIA PHARMS INC |
| Dosage forms | SOLUTION, INTRAVENOUS |
| Strength | 10%;10% (5GM/50ML;5GM/50ML) |
| Marketing status | Prescription |
| TE codes | AP |
| Reference listed drug | No |
| Latest submission status date | May 8, 2017 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- 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: