PMA supplement
P850037 S001: SODIUM CHLORIDE TABLETS, USP
FDA PMA supplement · Akorn, Inc.
Key facts
| Original PMA | P850037 |
|---|---|
| Supplement number | S001 |
| Trade name | SODIUM CHLORIDE TABLETS, USP |
| Generic name | Accessories, soft lens products |
| Applicant | Akorn, Inc. |
| Product code | LPN |
| Received date | Apr 1, 1986 |
| Decision date | Jun 9, 1986 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: