NDC 0615-8332 – Glimepiride

Glimepiride 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0615-8332

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091220
Marketed since
June 13, 2013
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (1)

Package NDCDescriptionSince
0615-8332-3930 TABLET in 1 BLISTER PACK (0615-8332-39)Apr 10, 2020

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