# ganciclovir sodium

NDC: 70436-231
Generic name: ganciclovir sodium
Labeler / Manufacturer: Slate Run Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20190101

FDA application: ANDA204204

## Active ingredients

- GANCICLOVIR SODIUM: 500 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70436-231"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70436-231
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cd293b9d-b573-4656-8574-19d7db870a9b