FDA NDC Directory · JSON-LD · Markdown

POSACONAZOLE

NDC 0904-7149 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA213454
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPOSACONAZOLE (100 mg/1)
Marketing started20210203
Package count2

External sources

Source: openFDA. Public-domain (CC0).