# Minocycline hydrochloride

NDC: 82868-017
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: 20231004

FDA application: ANDA063009

## 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:"82868-017"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82868-017
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0760232b-21a6-2b13-e063-6394a90a22c1