# Valacyclovir

NDC: 69117-0011
Generic name: Valacyclovir Hydrochloride
Labeler / Manufacturer: Yiling Pharmaceutical, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20181001

FDA application: ANDA209553

## Active ingredients

- VALACYCLOVIR HYDROCHLORIDE: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69117-0011"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69117-0011
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f3ee4017-a4fc-475d-a49b-b39168ec5966