# Minocycline Hydrochloride

NDC: 55289-201
Generic name: Minocycline Hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 19930501

FDA application: ANDA063065

## 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:"55289-201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55289-201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87a137c6-dd53-44d3-ab49-ef78ebed35c8