# Minocycline Hydrochloride

NDC: 62135-889
Generic name: Minocycline Hydrochloride
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20071226

FDA application: ANDA065436

## 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:"62135-889"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-889
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=43fbe7ff-4b67-474d-bf27-e5710d8d10ac