FDA NDC Directory · JSON-LD · Markdown

Tranexamic Acid

NDC 72319-028 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / Manufactureri3 Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA219702
Dosage form / routeTABLET · ORAL
Active ingredientsTRANEXAMIC ACID (650 mg/1)
Marketing started20260630
Package count1

External sources

Source: openFDA. Public-domain (CC0).