# Valacyclovir hydrochloride

NDC: 68788-6896
Generic name: Valacyclovir hydrochloride
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170213

FDA application: ANDA077135

## 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:"68788-6896"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-6896
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c153155b-69dc-41b7-91d2-0949ec496174