# minocycline hydrochloride

NDC: 68382-552
Generic name: minocycline hydrochloride
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20180307

FDA application: ANDA203553

## Active ingredients

- MINOCYCLINE HYDROCHLORIDE: 105 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68382-552"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-552
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=85f082a5-bba1-4441-ba28-4b8ec9a537f2