# Doxycycline

NDC: 31722-371
Generic name: Doxycycline
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250805

FDA application: ANDA218888

## Active ingredients

- DOXYCYCLINE HYCLATE: 100 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-371"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-371
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0faee97d-2707-48fe-a739-143cd1a1c4e3