# Valacyclovir

NDC: 31722-705
Generic name: Valacyclovir
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20150525

FDA application: ANDA203047

## 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:"31722-705"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-705
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7f5e96e0-534c-47a5-bb79-926088afc73c