FDA NDC Directory · JSON-LD · Markdown

Sodium Phenylbutyrate

NDC 42794-086 · HUMAN PRESCRIPTION DRUG · POWDER

Labeler / ManufacturerSigmapharm Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202819
Dosage form / routePOWDER · ORAL
Active ingredientsSODIUM PHENYLBUTYRATE (.94 g/g)
Marketing started20130408
Package count1

External sources

Source: openFDA. Public-domain (CC0).