NDC 68788-8512 – Glipizide

Glipizide 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8512

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074223
Marketed since
August 25, 2023
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8512-1100 TABLET in 1 BOTTLE, PLASTIC (68788-8512-1)Aug 25, 2023
68788-8512-330 TABLET in 1 BOTTLE, PLASTIC (68788-8512-3)Aug 25, 2023
68788-8512-660 TABLET in 1 BOTTLE, PLASTIC (68788-8512-6)Aug 25, 2023
68788-8512-8180 TABLET in 1 BOTTLE, PLASTIC (68788-8512-8)Aug 25, 2023
68788-8512-990 TABLET in 1 BOTTLE, PLASTIC (68788-8512-9)Aug 25, 2023

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