# valacyclovir hydrochloride

NDC: 59746-325
Generic name: valacyclovir hydrochloride
Labeler / Manufacturer: Jubilant Cadista Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120405

FDA application: ANDA201506

## 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:"59746-325"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59746-325
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3277c17e-f953-2b0a-fe0a-4f5d1aeace9d