# DOXYCYCLINE

NDC: 68180-657
Generic name: DOXYCYCLINE
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: FOR SUSPENSION
Routes: ORAL
Marketing started: 20130611

FDA application: ANDA201678

## Active ingredients

- DOXYCYCLINE: 25 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68180-657"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-657
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e0e80435-1b6a-4361-8c8a-e432f8f23a1b