FdaApplication
NDA 216018
Identifiers
- fda_app_no: NDA216018
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA INDUSTRIES LTD |
| application_type | NDA |
| approval_date | 2022-02-28 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ASPRUZYO SPRINKLE | RANOLAZINE | 500MG | GRANULE, EXTENDED RELEASE;ORAL |
| ASPRUZYO SPRINKLE | RANOLAZINE | 1GM | GRANULE, EXTENDED RELEASE;ORAL |
2 products