# Acyclovir

NDC: 63323-325
Generic name: acyclovir
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20001017

FDA application: ANDA074930

## Active ingredients

- ACYCLOVIR SODIUM: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-325"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-325
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=badf347b-eeee-4239-9c74-966f262925aa