# Minocycline Hydrochloride

NDC: 57664-852
Generic name: Minocycline Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20130513

FDA application: ANDA090867

## Active ingredients

- MINOCYCLINE HYDROCHLORIDE: 75 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57664-852"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-852
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ddd14292-3e39-4f2d-92f2-e7a6253f200a