FdaApplication
NDA 016801
Identifiers
- fda_app_no: NDA016801
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | NDA |
| approval_date | 1988-01-19 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| XYLOCAINE PRESERVATIVE FREE | LIDOCAINE HYDROCHLORIDE | 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| XYLOCAINE PRESERVATIVE FREE | LIDOCAINE HYDROCHLORIDE | 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| XYLOCAINE PRESERVATIVE FREE | LIDOCAINE HYDROCHLORIDE | 4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| XYLOCAINE PRESERVATIVE FREE | LIDOCAINE HYDROCHLORIDE | 10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| XYLOCAINE PRESERVATIVE FREE | LIDOCAINE HYDROCHLORIDE | 20% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
5 products