NDC 64980-281 – Glipizide

Glipizide 10 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC64980-281

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204720
Marketed since
April 24, 2017
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (3)

Package NDCDescriptionSince
64980-281-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64980-281-01)Apr 24, 2017
64980-281-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64980-281-05)Apr 24, 2017
64980-281-101000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64980-281-10)Apr 24, 2017

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