Drug application
TIAMATE (DILTIAZEM MALATE)
Drugs@FDA NDA 020506 · MERCK
Key facts
| Drug name | TIAMATE |
|---|---|
| Active ingredients | DILTIAZEM MALATE |
| Application type | NDA |
| Application number | 020506 |
| Company | MERCK |
| Dosage forms | TABLET, EXTENDED RELEASE, ORAL |
| Strength | EQ 120MG HYDROCHLORIDE |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission class | Type 2 - New Active Ingredient |
| Latest submission status date | Oct 4, 1996 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.