FdaApplication
NDA 020092
Identifiers
- fda_app_no: NDA020092
Properties
| Property | Value |
|---|---|
| applicant_name | ALLERGAN SALES LLC |
| application_type | NDA |
| approval_date | 1992-05-29 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DILACOR XR | DILTIAZEM HYDROCHLORIDE | 180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE, EXTENDED RELEASE;ORAL |
| DILACOR XR | DILTIAZEM HYDROCHLORIDE | 240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE, EXTENDED RELEASE;ORAL |
| DILACOR XR | DILTIAZEM HYDROCHLORIDE | 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE, EXTENDED RELEASE;ORAL |
3 products