NDC 82804-959 – Glipizide

Glipizide 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-959

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074378
Marketed since
May 1, 2025
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (7)

Package NDCDescriptionSince
82804-959-00100 TABLET in 1 BOTTLE (82804-959-00)Jan 12, 2026
82804-959-111000 TABLET in 1 BOTTLE (82804-959-11)Jan 12, 2026
82804-959-3030 TABLET in 1 BOTTLE (82804-959-30)Jan 12, 2026
82804-959-55500 TABLET in 1 BOTTLE (82804-959-55)Jan 12, 2026
82804-959-6060 TABLET in 1 BOTTLE (82804-959-60)Jan 12, 2026
82804-959-72120 TABLET in 1 BOTTLE (82804-959-72)Jan 12, 2026
82804-959-9090 TABLET in 1 BOTTLE (82804-959-90)Jan 12, 2026

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