# Acyclovir

NDC: 51655-679
Generic name: Acyclovir
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230215

FDA application: ANDA203834

## Active ingredients

- ACYCLOVIR: 800 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-679"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-679
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6f56143-ea74-af87-e053-6394a90ae346