Drug application
ZANTAC (RANITIDINE HYDROCHLORIDE)
Drugs@FDA NDA 019090 · PAI HOLDINGS PHARM
Key facts
| Drug name | ZANTAC |
|---|---|
| Active ingredients | RANITIDINE HYDROCHLORIDE |
| Application type | NDA |
| Application number | 019090 |
| Company | PAI HOLDINGS PHARM |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | EQ 25MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
| Marketing status | Discontinued |
| TE codes | AP |
| Reference listed drug | Yes |
| Latest submission class | Type 3 - New Dosage Form |
| Latest submission status date | Oct 19, 1984 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 1–9 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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: