FDA NDC Directory · JSON-LD · Markdown

Tretinoin

NDC 10370-268 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPar Health USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA201687
Dosage form / routeCAPSULE · ORAL
Active ingredientsTRETINOIN (10 mg/1)
Marketing started20121024
Package count1

External sources

Source: openFDA. Public-domain (CC0).