# Minocycline Hydrochloride

NDC: 68180-381
Generic name: Minocycline Hydrochloride
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20120214

FDA application: ANDA091424

## 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:"68180-381"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-381
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3b1e1cf1-ebd2-4aba-a219-9f9939fdb03b