Drug application
NICOTINE POLACRILEX (NICOTINE POLACRILEX)
Drugs@FDA ANDA 074707 · P AND L
Key facts
| Drug name | NICOTINE POLACRILEX |
|---|---|
| Active ingredients | NICOTINE POLACRILEX |
| Application type | ANDA |
| Application number | 074707 |
| Company | P AND L |
| Dosage forms | GUM, CHEWING, BUCCAL |
| Strength | EQ 4MG BASE |
| Marketing status | Over-the-counter |
| Reference listed drug | No |
| Latest submission status date | Mar 19, 1999 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 1–9 Label versions
- 1–9 Products
- None Therapeutic equivalents
- Yes FDA letters on file
- Yes FDA reviews on file
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: