NDC 68788-8487 – Glipizide

Glipizide 2.5 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC68788-8487

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204720
Marketed since
July 19, 2023
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8487-1100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8487-1)Jul 19, 2023
68788-8487-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8487-3)Jul 19, 2023
68788-8487-660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8487-6)Jul 19, 2023
68788-8487-990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-8487-9)Jul 19, 2023

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