Glipizide

Product NDC
65862-890
11-digit product format
658620890
Labeler code
65862
Product ID
65862-890_963bea5a-dda1-4ce0-9ee4-35e40eb82606
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glipizide
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Aurobindo Pharma Limited
Application
ANDA206928
Marketing category
ANDA
Marketing start
2017-05-12
Marketing end
2020-09-30
Substance
GLIPIZIDE
Active strength
10 mg/1
Pharmacologic classes
Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ec4adfb0-aabc-95b9-ad07-5cb8f8533a09Product name220250625
b1de1ca9-d9db-4f4b-2103-09e2014d30d5Product name520180912
2dee091b-3b8c-d27a-b1ba-fcb0d32e776aProduct name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
65862-890-01EA - Each65862-8907d561a82-8812-4955-9e1f-bc3ee69fe15d12018-01-12

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
315107glipiZIDE 10 MG 24HR Extended Release Oral TabletPSN0af8dc45-9595-4fc8-8198-0ac59523279f2
31510724 HR glipizide 10 MG Extended Release Oral TabletSCD0af8dc45-9595-4fc8-8198-0ac59523279f2
315107glipizide ER 10 MG 24 HR Extended Release Oral TabletSY0af8dc45-9595-4fc8-8198-0ac59523279f2
315107glipizide XL 10 MG 24 HR Extended Release Oral TabletSY0af8dc45-9595-4fc8-8198-0ac59523279f2