FdaApplication
ANDA 084361
Identifiers
- fda_app_no: ANDA084361
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1986-02-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DICYCLOMINE HYDROCHLORIDE | DICYCLOMINE HYDROCHLORIDE | 20MG | TABLET;ORAL |
1 product