FDA NDC Directory · JSON-LD · Markdown

SILODOSIN

NDC 72789-351 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210626
Dosage form / routeCAPSULE · ORAL
Active ingredientsSILODOSIN (4 mg/1)
Marketing started20181210
Package count1

External sources

Source: openFDA. Public-domain (CC0).