FDA NDC Directory · JSON-LD · Markdown

Phenobarbital

NDC 67046-0059 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCoupler LLC
Marketing categoryUnapproved drug (not FDA-reviewed)
Dosage form / routeTABLET · ORAL
Active ingredientsPHENOBARBITAL (32.4 mg/1)
Marketing started20260622
Package count1

External sources

Source: openFDA. Public-domain (CC0).