Glipizide

Product NDC
50090-4911
11-digit product format
500904911
Labeler code
50090
Product ID
50090-4911_c99f0a64-95b2-4dfa-a977-b9778d80f9ab
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glipizide
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA206928
Marketing category
ANDA
Marketing start
2017-05-12
Marketing end
0000-00-00
Substance
GLIPIZIDE
Active strength
10 mg/1
Pharmacologic classes
Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
X7WDT95N5CGLIPIZIDE29094-61-9GLIPIZIDE

Packages

Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-4911-05009049110030 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4911-0) 2020-02-180000-00-00NoNoCurrent
50090-4911-15009049110160 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4911-1) 2020-02-180000-00-00NoNoCurrent
50090-4911-25009049110290 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4911-2) 2020-02-180000-00-00NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
GlipizideA-S Medication Solutions2020-02-25Human Prescription Drug Label1