# DOXYCYCLINE

NDC: 42023-244
Generic name: Doxycycline
Labeler / Manufacturer: Par Health USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20241126

FDA application: ANDA216690

## 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:"42023-244"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42023-244
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=acb84610-5e26-4b0c-89e5-42bc0f8fa00d