Drug application
RANITIDINE HYDROCHLORIDE (RANITIDINE HYDROCHLORIDE)
Drugs@FDA ANDA 077405 · PHARM ASSOC
Key facts
| Drug name | RANITIDINE HYDROCHLORIDE |
|---|---|
| Active ingredients | RANITIDINE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 077405 |
| Company | PHARM ASSOC |
| Dosage forms | SYRUP, ORAL |
| Strength | EQ 15MG BASE/ML |
| Marketing status | Discontinued |
| TE codes | AA |
| Reference listed drug | No |
| Latest submission status date | Sep 21, 2007 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- 1–9 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.