# OXYCODONE HYDROCHLORIDE
> **ANDA212429** · Abbreviated New Drug Application (Generic) · Sponsor: AUROLIFE PHARMA LLC · Approved 2020-01-27
## Drug
- **FDA Application Number:** ANDA212429
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** OXYCODONE HYDROCHLORIDE
- **Generic name:** OXYCODONE HYDROCHLORIDE ORAL SOLUTION
- **Active ingredients:** OXYCODONE HYDROCHLORIDE
- **Dosage form:** SOLUTION
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** AUROLIFE PHARMA LLC
- **Manufacturer:** Aurolife Pharma, LLC
- **First approval:** 2020-01-27
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=212429)
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