FdaApplication
ANDA 210948
Identifiers
- fda_app_no: ANDA210948
Properties
| Property | Value |
|---|---|
| applicant_name | AIZANT DRUG RESEARCH SOLUTIONS PRIVATE LTD |
| application_type | ANDA |
| approval_date | 2019-03-15 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 4MG BASE | TABLET;ORAL |
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 2MG BASE | TABLET;ORAL |
2 products