FDA NDC Directory · JSON-LD · Markdown

Thiotepa

NDC 43598-650 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerDr.Reddy's Laboratories Inc.,
Marketing categoryAbbreviated NDA (generic) · App ANDA210337
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRACAVITARY INTRAVENOUS INTRAVESICAL
Active ingredientsTHIOTEPA (15 mg/1)
Marketing started20180504
Package count1

External sources

Source: openFDA. Public-domain (CC0).