FdaApplication
ANDA 215342
Identifiers
- fda_app_no: ANDA215342
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2022-01-26 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ATROPINE SULFATE | ATROPINE SULFATE | 1MG/10ML (0.1MG/ML) | SOLUTION;INTRAVENOUS |
| ATROPINE SULFATE | ATROPINE SULFATE | 0.5MG/5ML (0.1MG/ML) | SOLUTION;INTRAVENOUS |
2 products