Drug application
NORLESTRIN 21 1/50 (ETHINYL ESTRADIOL, NORETHINDRONE ACETATE)
Drugs@FDA NDA 016749 · PARKE DAVIS
Key facts
| Drug name | NORLESTRIN 21 1/50 |
|---|---|
| Active ingredients | ETHINYL ESTRADIOL, NORETHINDRONE ACETATE |
| Application type | NDA |
| Application number | 016749 |
| Company | PARKE DAVIS |
| Dosage forms | TABLET, ORAL-21 |
| Strength | 0.05MG;1MG |
| Marketing status | Discontinued |
| Reference listed drug | No |
At a glance
- 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.