FdaApplication
ANDA 078652
Identifiers
- fda_app_no: ANDA078652
Properties
| Property | Value |
|---|---|
| applicant_name | ZYDUS PHARMS USA INC |
| application_type | ANDA |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE | 5MG;20MG | CAPSULE;ORAL |
| AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE | 5MG;10MG | CAPSULE;ORAL |
| AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE | 2.5MG;10MG | CAPSULE;ORAL |
| AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE | 10MG;20MG | CAPSULE;ORAL |
4 products