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Thiotepa

NDC 43598-171 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerDr.Reddy's Laboratories Inc.,
Marketing categoryAbbreviated NDA (generic) · App ANDA214222
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRACAVITARY INTRAVENOUS INTRAVESICAL
Active ingredientsTHIOTEPA (100 mg/1)
Marketing started20221101
Package count1

External sources

Source: openFDA. Public-domain (CC0).