# Minocycline Hydrochloride

NDC: 51655-004
Generic name: Minocycline Hydrochloride
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20140820

FDA application: ANDA065470

## Active ingredients

- MINOCYCLINE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-004"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-004
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=12559b29-6568-4b99-a16e-6a87038981f7