NDC 0093-8035 – Glyburide

Glyburide 3 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0093-8035

Product details

Brand name
Glyburide
Generic name
Glyburide
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074686
Marketed since
May 11, 1999
Marketing end
January 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glyburide →

Package NDC codes (2)

Package NDCDescriptionSince
0093-8035-01100 TABLET in 1 BOTTLE (0093-8035-01)May 11, 1999
0093-8035-05500 TABLET in 1 BOTTLE (0093-8035-05)May 11, 1999

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