# Minocycline hydrochloride

NDC: 80425-0314
Generic name: Minocycline hydrochloride
Labeler / Manufacturer: Advanced Rx Pharmacy of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20230410

FDA application: ANDA065062

## 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:"80425-0314"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0314
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f901a1ba-1716-8795-e053-6294a90a4e77