FdaApplication
ANDA 216552
Identifiers
- fda_app_no: ANDA216552
Properties
| Property | Value |
|---|---|
| applicant_name | EUGIA PHARMA SPECIALITIES LTD |
| application_type | ANDA |
| approval_date | 2023-03-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DILTIAZEM HYDROCHLORIDE | DILTIAZEM HYDROCHLORIDE | 5MG/ML | INJECTABLE;INJECTION |
1 product