FdaApplication
ANDA 073529
Identifiers
- fda_app_no: ANDA073529
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1992-01-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DOXAPRAM HYDROCHLORIDE | DOXAPRAM HYDROCHLORIDE | 20MG/ML | INJECTABLE;INJECTION |
1 product