FDA NDC Directory · JSON-LD · Markdown

Nintedanib

NDC 42799-973 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namenintedanib
Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA219819
Dosage form / routeCAPSULE · ORAL
Active ingredientsNINTEDANIB ESYLATE (150 mg/1)
Marketing started20260403
Package count1

External sources

Source: openFDA. Public-domain (CC0).