FdaApplication
NDA 016793
Identifiers
- fda_app_no: NDA016793
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PARENTERAL MEDICINES INC |
| application_type | NDA |
| approval_date | 1987-12-21 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CYTARABINE | CYTARABINE | 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| CYTARABINE | CYTARABINE | 100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| CYTARABINE | CYTARABINE | 1GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| CYTARABINE | CYTARABINE | 2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
4 products