FDA NDC Directory · JSON-LD · Markdown

Glimepiride

NDC 71921-216 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerFlorida Pharmaceutical Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202112
Dosage form / routeTABLET · ORAL
Active ingredientsGLIMEPIRIDE (4 mg/1)
Marketing started20230731
Package count2

External sources

Source: openFDA. Public-domain (CC0).