# Minocycline Hydrochloride

NDC: 59651-337
Generic name: Minocycline Hydrochloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200501

FDA application: ANDA213662

## Active ingredients

- MINOCYCLINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-337"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-337
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=799a9871-3249-471e-b88d-5d8f7d4b96ad