Glyburide

Product NDC
63629-1393
11-digit product format
636291393
Labeler code
63629
Product ID
63629-1393_01c04386-c1d5-4fd9-bb05-37caf64516de
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glyburide
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA074388
Marketing category
ANDA
Marketing start
1995-08-30
Marketing end
0000-00-00
Substance
GLYBURIDE
Active strength
5 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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-1393-1EA - Each63629-1393d0bf62c8-da35-4fd7-8aef-8374fa30da9212013-02-13
63629-1393-2EA - Each63629-13938c6a594b-a719-4673-b78f-65ab29cce51f12013-02-13
63629-1393-3EA - Each63629-139331125f44-3702-4c40-9048-92b3a40d572312013-02-13
63629-1393-4EA - Each63629-1393b5c3fe63-7a4d-4ad6-8345-f8cd4c76a52312015-10-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-1393-16362913930130 TABLET in 1 BOTTLE (63629-1393-1) 30 tablet1995-08-300000-00-00NoNoCurrent
63629-1393-263629139302120 TABLET in 1 BOTTLE (63629-1393-2) 120 tablet1995-08-300000-00-00NoNoCurrent
63629-1393-363629139303100 TABLET in 1 BOTTLE (63629-1393-3) 100 tablet1995-08-300000-00-00NoNoCurrent
63629-1393-46362913930460 TABLET in 1 BOTTLE (63629-1393-4) 60 tablet1995-08-300000-00-00NoNoCurrent
63629-1393-56362913930590 TABLET in 1 BOTTLE (63629-1393-5) 90 tablet1995-08-300000-00-00NoNoCurrent
63629-1393-663629139306180 TABLET in 1 BOTTLE (63629-1393-6) 180 tablet1995-08-300000-00-00NoNoCurrent