FdaApplication
ANDA 202651
Identifiers
- fda_app_no: ANDA202651
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA FARMACEUTICA PORTUGAL SA |
| application_type | ANDA |
| approval_date | 2012-08-09 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DILTIAZEM HYDROCHLORIDE | DILTIAZEM HYDROCHLORIDE | 5MG/ML | INJECTABLE;INJECTION |
| DILTIAZEM HYDROCHLORIDE | DILTIAZEM HYDROCHLORIDE | 50MG/10ML | INJECTABLE;INJECTION |
| DILTIAZEM HYDROCHLORIDE | DILTIAZEM HYDROCHLORIDE | 125MG/25ML | INJECTABLE;INJECTION |
3 products