FDA NDC Directory · JSON-LD · Markdown

ganciclovir sodium

NDC 70436-231 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerSlate Run Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204204
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsGANCICLOVIR SODIUM (500 mg/10mL)
Marketing started20190101
Package count1

External sources

Source: openFDA. Public-domain (CC0).