# Doxycycline

NDC: 0527-1535
Generic name: Doxycycline
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20080825

FDA application: ANDA065285

## Active ingredients

- DOXYCYCLINE: 75 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0527-1535"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0527-1535
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4999bbd9-44ed-4749-9730-be2337bdf490