NDC 0093-8342 – Glyburide

Glyburide 1.25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0093-8342

Product details

Brand name
Glyburide
Generic name
Glyburide
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074388
Marketed since
August 30, 1995
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glyburide →

Package NDC codes (1)

Package NDCDescriptionSince
0093-8342-01100 TABLET in 1 BOTTLE (0093-8342-01)Aug 30, 1995

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