FDA NDC Directory · JSON-LD · Markdown

Tretinoin

NDC 68084-075 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA201687
Dosage form / routeCAPSULE · ORAL
Active ingredientsTRETINOIN (10 mg/1)
Marketing started20130718
Package count1

External sources

Source: openFDA. Public-domain (CC0).