Glipizide

Product NDC
10370-746
11-digit product format
103700746
Labeler code
10370
Product ID
10370-746_dc569df1-efda-489d-b287-36e1a94fe09c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glipizide
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Par Pharmaceutical, Inc.
Application
ANDA076159
Marketing category
ANDA
Marketing start
2016-12-21
Marketing end
0000-00-00
Substance
GLIPIZIDE
Active strength
10 mg/1
Pharmacologic classes
Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ec4adfb0-aabc-95b9-ad07-5cb8f8533a09Product name220250625
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
b1de1ca9-d9db-4f4b-2103-09e2014d30d5Product name520180912
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
2dee091b-3b8c-d27a-b1ba-fcb0d32e776aProduct name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10370-746-01EA - Each10370-746dc823a10-afc7-460e-991b-76142a4e6ca912017-03-06
10370-746-05EA - Each10370-7466248d879-0d2b-4126-9756-d969692c9da512017-03-06

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
315107glipiZIDE 10 MG 24HR Extended Release Oral TabletPSN98591ff5-b735-47b0-9bd2-1e9118d261e610
314006glipiZIDE 5 MG 24HR Extended Release Oral TabletPSN98591ff5-b735-47b0-9bd2-1e9118d261e610
31510724 HR glipizide 10 MG Extended Release Oral TabletSCD98591ff5-b735-47b0-9bd2-1e9118d261e610
31400624 HR glipizide 5 MG Extended Release Oral TabletSCD98591ff5-b735-47b0-9bd2-1e9118d261e610
315107glipizide ER 10 MG 24 HR Extended Release Oral TabletSY98591ff5-b735-47b0-9bd2-1e9118d261e610
314006glipizide ER 5 MG 24 HR Extended Release Oral TabletSY98591ff5-b735-47b0-9bd2-1e9118d261e610
315107glipizide XL 10 MG 24 HR Extended Release Oral TabletSY98591ff5-b735-47b0-9bd2-1e9118d261e610
314006glipizide XL 5 MG 24 HR Extended Release Oral TabletSY98591ff5-b735-47b0-9bd2-1e9118d261e610
315107glipiZIDE 10 MG 24HR Extended Release Oral TabletPSN999d353d-ef88-45fb-8df9-572c0d2bb1e27
31510724 HR glipizide 10 MG Extended Release Oral TabletSCD999d353d-ef88-45fb-8df9-572c0d2bb1e27
315107glipizide ER 10 MG 24 HR Extended Release Oral TabletSY999d353d-ef88-45fb-8df9-572c0d2bb1e27
315107glipizide XL 10 MG 24 HR Extended Release Oral TabletSY999d353d-ef88-45fb-8df9-572c0d2bb1e27
315107glipiZIDE 10 MG 24HR Extended Release Oral TabletPSN0fa9b09f-27d1-4092-87d7-32ec374518473
31510724 HR glipizide 10 MG Extended Release Oral TabletSCD0fa9b09f-27d1-4092-87d7-32ec374518473
315107glipizide ER 10 MG 24 HR Extended Release Oral TabletSY0fa9b09f-27d1-4092-87d7-32ec374518473
315107glipizide XL 10 MG 24 HR Extended Release Oral TabletSY0fa9b09f-27d1-4092-87d7-32ec374518473

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
10370-746-0110370074601100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-746-01) 2017-04-250000-00-00NoNoCurrent
10370-746-0510370074605500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-746-05) 2017-01-240000-00-00NoNoCurrent