Drug application
HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.9% (HEPARIN SODIUM)
Drugs@FDA NDA 018916 · HOSPIRA
Key facts
| Drug name | HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.9% |
|---|---|
| Active ingredients | HEPARIN SODIUM |
| Application type | NDA |
| Application number | 018916 |
| Company | HOSPIRA |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | 1,000 UNITS/100ML |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission class | Type 5 - New Formulation or New Manufacturer |
| Latest submission status date | Jan 31, 1984 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 1–9 Label versions
- 10–99 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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: