# Doxycycline

NDC: 70771-1122
Generic name: Doxycycline
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20180201

FDA application: ANDA207757

## Active ingredients

- DOXYCYCLINE HYCLATE: 200 mg/20mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1122"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1122
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6ae11b4e-1c13-440b-a050-d76e062b0f92