FdaApplication
ANDA 075114
Identifiers
- fda_app_no: ANDA075114
Properties
| Property | Value |
|---|---|
| applicant_name | ABBVIE INC |
| application_type | ANDA |
| approval_date | 1999-07-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ACYCLOVIR | ACYCLOVIR SODIUM | EQ 50MG BASE/ML | INJECTABLE;INJECTION |
1 product