# Doxycycline

NDC: 63304-173
Generic name: Doxycycline
Labeler / Manufacturer: Sun Pharmaceutical Industries Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180806

FDA application: ANDA065356

## Active ingredients

- DOXYCYCLINE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63304-173"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63304-173
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8224b9c5-5c4b-4dda-bc58-47b6604c2884