NDC 71921-216 – Glimepiride

Glimepiride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71921-216

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Florida Pharmaceutical Products, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202112
Marketed since
July 31, 2023
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (2)

Package NDCDescriptionSince
71921-216-01100 TABLET in 1 BOTTLE (71921-216-01)Jul 31, 2023
71921-216-50500 TABLET in 1 BOTTLE (71921-216-50)Jul 31, 2023

Other Glimepiride products