NDC 68382-656 – glyburide

Glyburide 1.25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-656

Product details

Brand name
glyburide
Generic name
glyburide
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206749
Marketed since
June 2, 2016
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glyburide →

Package NDC codes (6)

Package NDCDescriptionSince
68382-656-01100 TABLET in 1 BOTTLE (68382-656-01)Jun 2, 2016
68382-656-05500 TABLET in 1 BOTTLE (68382-656-05)Jun 2, 2016
68382-656-0630 TABLET in 1 BOTTLE (68382-656-06)Jun 2, 2016
68382-656-101000 TABLET in 1 BOTTLE (68382-656-10)Jun 2, 2016
68382-656-1690 TABLET in 1 BOTTLE (68382-656-16)Jun 2, 2016
68382-656-7710 BLISTER PACK in 1 CARTON (68382-656-77) / 10 TABLET in 1 BLISTER PACK (68382-656-30)Jun 2, 2016

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