# AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
> **ANDA077179** · Abbreviated New Drug Application (Generic) · Sponsor: TEVA PHARMS · Approved 2007-05-18
## Drug
- **FDA Application Number:** ANDA077179
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
- **Generic name:** Amlodipine Besylate
- **Active ingredients:** AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
- **Dosage form:** CAPSULE
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** TEVA PHARMS
- **First approval:** 2007-05-18
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=077179)
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