# DOXYCYCLINE

NDC: 0404-9855
Generic name: doxycycline
Labeler / Manufacturer: Henry Schein, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220110
Marketing ended: 20270331
FDA application: ANDA091406

## 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:"0404-9855"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0404-9855
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dd70368b-1949-4833-9d1e-f9f4cdacd9f3