FDA NDC Directory · JSON-LD · Markdown

Acitretin

NDC 0093-1138 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202897
Dosage form / routeCAPSULE · ORAL
Active ingredientsACITRETIN (17.5 mg/1)
Marketing started20130719
Package count1

External sources

Source: openFDA. Public-domain (CC0).