FDA NDC Directory · JSON-LD · Markdown

MYHIBBIN

NDC 24338-018 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Generic nameMYCOPHENOLATE MOFETIL
Labeler / ManufacturerAzurity Pharmaceuticals, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA216482
Dosage form / routeSUSPENSION · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (200 mg/mL)
Marketing started20240610
Package count1

External sources

Source: openFDA. Public-domain (CC0).