Drug application
NICOTINE (NICOTINE)
Drugs@FDA ANDA 074612 · DIFGEN PHARMS
Key facts
| Drug name | NICOTINE |
|---|---|
| Active ingredients | NICOTINE |
| Application type | ANDA |
| Application number | 074612 |
| Company | DIFGEN PHARMS |
| Dosage forms | FILM, EXTENDED RELEASE, TRANSDERMAL |
| Strength | 21MG/24HR |
| Marketing status | Over-the-counter |
| Reference listed drug | No |
| Latest submission status date | Oct 20, 1997 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 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.