FdaApplication
ANDA 070841
Identifiers
- fda_app_no: ANDA070841
Properties
| Property | Value |
|---|---|
| applicant_name | SMITH AND NEPHEW SOLOPAK DIV SMITH AND NEPHEW |
| application_type | ANDA |
| approval_date | 1987-01-02 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHYLDOPATE HYDROCHLORIDE | METHYLDOPATE HYDROCHLORIDE | 50MG/ML | INJECTABLE;INJECTION |
1 product