# Valacyclovir Hydrochloride

NDC: 71335-1341
Generic name: Valacyclovir Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20100524

FDA application: ANDA078518

## Active ingredients

- VALACYCLOVIR HYDROCHLORIDE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-1341"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-1341
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c28c069f-3b51-4474-aa38-1aed6b7b8678