# Doxycycline

NDC: 70710-1122
Generic name: Doxycycline
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180111

FDA application: ANDA209582

## Active ingredients

- DOXYCYCLINE: 75 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1122"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1122
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bc321932-b600-4659-a499-1853991b4ab9