# Minocycline Hydrochloride

NDC: 70518-1336
Generic name: Minocycline Hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20180801

FDA application: ANDA065470

## Active ingredients

- MINOCYCLINE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-1336"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-1336
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0becbde8-6ec5-4830-a0d9-cfdb7b15eb84