FdaApplication
NDA 018304
Identifiers
- fda_app_no: NDA018304
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | NDA |
| approval_date | 1983-09-02 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SENSORCAINE | BUPIVACAINE HYDROCHLORIDE; EPINEPHRINE BITARTRATE | 0.75%;0.0091MG/ML | INJECTABLE;INJECTION |
| SENSORCAINE | BUPIVACAINE HYDROCHLORIDE; EPINEPHRINE BITARTRATE | 0.5%;0.0091MG/ML | INJECTABLE;INJECTION |
| SENSORCAINE | BUPIVACAINE HYDROCHLORIDE | 0.75% | INJECTABLE;INJECTION |
| SENSORCAINE | BUPIVACAINE HYDROCHLORIDE | 0.25% | INJECTABLE;INJECTION |
| SENSORCAINE | BUPIVACAINE HYDROCHLORIDE | 0.5% | INJECTABLE;INJECTION |
5 products