# Minocin

NDC: 70842-160
Generic name: minocycline hydrochloride
Labeler / Manufacturer: Melinta Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20130419

FDA application: NDA050444

## Active ingredients

- MINOCYCLINE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70842-160"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70842-160
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e415c323-8219-464b-9e3e-72c5a796cdaa