FdaApplication
NDA 020577
Identifiers
- fda_app_no: NDA020577
Properties
| Property | Value |
|---|---|
| applicant_name | LUKARE MEDICAL LLC |
| application_type | NDA |
| approval_date | 1996-09-27 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ELLIOTTS B SOLUTION | CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE | 0.2MG/ML;0.8MG/ML;0.3MG/ML;0.3MG/ML;1.9MG/ML;7.3MG/ML;0.2MG/ML | INJECTABLE;INTRATHECAL |
1 product