Drug application
RANITIDINE (RANITIDINE)
Drugs@FDA ANDA 074794 · ACTAVIS ELIZABETH
Key facts
| Drug name | RANITIDINE |
|---|---|
| Active ingredients | RANITIDINE |
| Application type | ANDA |
| Application number | 074794 |
| Company | ACTAVIS ELIZABETH |
| Dosage forms | Solution, Oral |
| Strength | 15MG/ML |
| Marketing status | None (Tentative Approval) |
| Reference listed drug | No |
| Latest submission status date | Nov 18, 1997 |
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.