NDC 50090-7406 – Glimepiride

Glimepiride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-7406

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
A-S Medication Solutions
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 (5)

Package NDCDescriptionSince
50090-7406-030 TABLET in 1 BOTTLE (50090-7406-0)Oct 24, 2024
50090-7406-1100 TABLET in 1 BOTTLE (50090-7406-1)Oct 24, 2024
50090-7406-260 TABLET in 1 BOTTLE (50090-7406-2)Oct 24, 2024
50090-7406-390 TABLET in 1 BOTTLE (50090-7406-3)Oct 24, 2024
50090-7406-4180 TABLET in 1 BOTTLE (50090-7406-4)Oct 24, 2024

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