NDC 71205-773 – Glimepiride

Glimepiride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-773

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202759
Marketed since
June 29, 2012
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (4)

Package NDCDescriptionSince
71205-773-3030 TABLET in 1 BOTTLE (71205-773-30)Mar 13, 2023
71205-773-6060 TABLET in 1 BOTTLE (71205-773-60)Mar 13, 2023
71205-773-78180 TABLET in 1 BOTTLE (71205-773-78)Mar 13, 2023
71205-773-9090 TABLET in 1 BOTTLE (71205-773-90)Mar 13, 2023

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