# Minocycline Hydrochloride

NDC: 65862-885
Generic name: Minocycline Hydrochloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160613

FDA application: ANDA202261

## Active ingredients

- MINOCYCLINE HYDROCHLORIDE: 105 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-885"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-885
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e7b88a48-12b3-461d-b356-0d7ae4e8fd44