NDC 68788-8138 – Glipizide

Glipizide 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8138

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Preferred Pharmaceuticals Inc..
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074223
Marketed since
February 11, 2022
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8138-1100 TABLET in 1 BOTTLE, PLASTIC (68788-8138-1)Feb 11, 2022
68788-8138-330 TABLET in 1 BOTTLE, PLASTIC (68788-8138-3)Feb 11, 2022
68788-8138-660 TABLET in 1 BOTTLE, PLASTIC (68788-8138-6)Feb 11, 2022
68788-8138-8180 TABLET in 1 BOTTLE, PLASTIC (68788-8138-8)Feb 11, 2022
68788-8138-990 TABLET in 1 BOTTLE, PLASTIC (68788-8138-9)Feb 11, 2022

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