# Minocycline Hydrochloride

NDC: 65862-211
Generic name: Minocycline Hydrochloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20080311

FDA application: ANDA065470

## 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:"65862-211"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-211
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9013ca48-15f2-43cd-a51d-91cf65c72a7c