FdaApplication
ANDA 209851
Identifiers
- fda_app_no: ANDA209851
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2022-05-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PEMETREXED DISODIUM | PEMETREXED DISODIUM | EQ 750MG BASE/VIAL | POWDER;INTRAVENOUS |
1 product