Home NDC 59762-5032 NDC 59762-5032 - Glipizide XL This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 59762-5032
Manufacturer State of Florida DOH Central Pharmacy
Effective date 2010-06-02
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded GLIPIZIDE ACTIVE INGREDIENT X7WDT95N5C GLIPIZIDE XL (GLIPIZIDE) TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY] 1 glipizide ACTIVE MOIETY X7WDT95N5C GLIPIZIDE XL (GLIPIZIDE) TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY] 1 CELLULOSE ACETATE INACTIVE INGREDIENT 3J2P07GVB6 GLIPIZIDE XL (GLIPIZIDE) TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY] 1 FERRIC OXIDE RED INACTIVE INGREDIENT 1K09F3G675 GLIPIZIDE XL (GLIPIZIDE) TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY] 1 HYPROMELLOSE INACTIVE INGREDIENT 3NXW29V3WO GLIPIZIDE XL (GLIPIZIDE) TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY] 1 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 GLIPIZIDE XL (GLIPIZIDE) TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY] 1 POLYETHYLENE GLYCOL INACTIVE INGREDIENT 3WJQ0SDW1A GLIPIZIDE XL (GLIPIZIDE) TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY] 1 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X GLIPIZIDE XL (GLIPIZIDE) TABLET, EXTENDED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY] 1