NDC 68071-2385 – Glimepiride

Glimepiride 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-2385

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077091
Marketed since
October 6, 2005
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (3)

Package NDCDescriptionSince
68071-2385-660 TABLET in 1 BOTTLE (68071-2385-6)Apr 9, 2021
68071-2385-8180 TABLET in 1 BOTTLE (68071-2385-8)Apr 9, 2021
68071-2385-990 TABLET in 1 BOTTLE (68071-2385-9)Apr 9, 2021

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