NDC 68001-584 – Glimepiride

Glimepiride 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68001-584

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
BluePoint Laboratories
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091220
Marketed since
September 1, 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
68001-584-00100 TABLET in 1 BOTTLE (68001-584-00)Sep 1, 2023
68001-584-03500 TABLET in 1 BOTTLE (68001-584-03)Sep 1, 2023

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