# MINOCIN
> **NDA050444** · New Drug Application · Sponsor: REMPEX · Approved 1972-10-26
## Drug
- **FDA Application Number:** NDA050444
- **Application type:** New Drug Application
- **Brand name:** MINOCIN
- **Generic name:** MINOCYCLINE HYDROCHLORIDE
- **Active ingredients:** MINOCYCLINE HYDROCHLORIDE
- **Dosage form:** INJECTABLE
- **Route:** INJECTION
- **Marketing status:** Prescription
- **Sponsor:** REMPEX
- **Manufacturer:** Melinta Therapeutics, LLC
- **First approval:** 1972-10-26
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=050444)
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