FdaApplication
NDA 212862
Identifiers
- fda_app_no: NDA212862
Properties
| Property | Value |
|---|---|
| applicant_name | MYLAN IRELAND LTD |
| application_type | NDA |
| approval_date | 2019-08-14 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PRETOMANID | PRETOMANID | 200MG | TABLET;ORAL |
1 product