# Minocycline Hydrochloride

NDC: 67877-577
Generic name: Minocycline Hydrochloride
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160930

FDA application: ANDA204453

## Active ingredients

- MINOCYCLINE HYDROCHLORIDE: 135 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-577"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-577
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a8f95207-b259-4f50-87f2-3652d9268890