# NALOXONE
> **ANDA070299** · Abbreviated New Drug Application (Generic) · Sponsor: HIKMA · Approved 1985-10-22
## Drug
- **FDA Application Number:** ANDA070299
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** NALOXONE
- **Generic name:** NALXONE HYDROCHLORIDE
- **Active ingredients:** NALOXONE HYDROCHLORIDE
- **Dosage form:** INJECTABLE
- **Route:** INJECTION
- **Marketing status:** Prescription
- **Sponsor:** HIKMA
- **Manufacturer:** Hikma Pharmaceuticals USA Inc.
- **First approval:** 1985-10-22
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=070299)
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