Drug application
ATROPINE SULFATE (ATROPINE SULFATE)
Drugs@FDA NDA 209260 · FRESENIUS KABI USA
Key facts
| Drug name | ATROPINE SULFATE |
|---|---|
| Active ingredients | ATROPINE SULFATE |
| Application type | NDA |
| Application number | 209260 |
| Company | FRESENIUS KABI USA |
| Dosage forms | SOLUTION, INTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS, INTRAOSSEOUS, ENDOTRACHEAL |
| Strength | 8MG/20ML (0.4MG/ML) |
| Marketing status | Prescription |
| TE codes | AP |
| Reference listed drug | Yes |
| Latest submission status date | Jan 26, 2018 |
At a glance
- 1–9 Submissions
- 1–9 Label versions
- 1–9 Products
- 1–9 Therapeutic equivalents
- Yes 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: