# Doxycycline

NDC: 71288-030
Generic name: Doxycycline
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20241028

FDA application: ANDA218053

## 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:"71288-030"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-030
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7772e702-20b3-473a-8bd5-9c7c92e753c6