# NEBIVOLOL HYDROCHLORIDE
> **ANDA211053** · Abbreviated New Drug Application (Generic) · Sponsor: AUROBINDO PHARMA LTD · Approved 2021-12-17
## Drug
- **FDA Application Number:** ANDA211053
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** NEBIVOLOL HYDROCHLORIDE
- **Generic name:** NEBIVOLOL
- **Active ingredients:** NEBIVOLOL HYDROCHLORIDE
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** AUROBINDO PHARMA LTD
- **Manufacturer:** Aurobindo Pharma Limited
- **First approval:** 2021-12-17
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=211053)
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