FDA NDC Directory · JSON-LD · Markdown

MYCOPHENOLIC ACID

NDC 70518-4391 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA208315
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsMYCOPHENOLATE SODIUM (360 mg/1)
Marketing started20250715
Package count1

External sources

Source: openFDA. Public-domain (CC0).