FdaApplication
ANDA 201722
Identifiers
- fda_app_no: ANDA201722
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | ANDA |
| approval_date | 2016-02-16 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NITROFURANTOIN | NITROFURANTOIN, MACROCRYSTALLINE | 50MG | CAPSULE;ORAL |
| NITROFURANTOIN | NITROFURANTOIN, MACROCRYSTALLINE | 100MG | CAPSULE;ORAL |
| NITROFURANTOIN | NITROFURANTOIN, MACROCRYSTALLINE | 25MG | CAPSULE;ORAL |
3 products