Prednisone

Product NDC
71335-1629
11-digit product format
713351629
Labeler code
71335
Product ID
71335-1629_2aed7717-1566-4913-b7cb-575320661a27
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prednisone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA085161
Marketing category
ANDA
Marketing start
1990-01-01
Marketing end
0000-00-00
Substance
PREDNISONE
Active strength
20 mg/1
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1629-07133516290011 TABLET in 1 BOTTLE (71335-1629-0) 11 tablet1990-01-010000-00-00NoNoCurrent
71335-1629-17133516290120 TABLET in 1 BOTTLE (71335-1629-1) 20 tablet1990-01-010000-00-00NoNoCurrent
71335-1629-27133516290230 TABLET in 1 BOTTLE (71335-1629-2) 30 tablet1990-01-010000-00-00NoNoCurrent
71335-1629-37133516290340 TABLET in 1 BOTTLE (71335-1629-3) 40 tablet1990-01-010000-00-00NoNoCurrent
71335-1629-47133516290415 TABLET in 1 BOTTLE (71335-1629-4) 15 tablet1990-01-010000-00-00NoNoCurrent
71335-1629-57133516290510 TABLET in 1 BOTTLE (71335-1629-5) 10 tablet1990-01-010000-00-00NoNoCurrent
71335-1629-67133516290621 TABLET in 1 BOTTLE (71335-1629-6) 21 tablet1990-01-010000-00-00NoNoCurrent
71335-1629-77133516290718 TABLET in 1 BOTTLE (71335-1629-7) 18 tablet1990-01-010000-00-00NoNoCurrent
71335-1629-87133516290812 TABLET in 1 BOTTLE (71335-1629-8) 12 tablet1990-01-010000-00-00NoNoCurrent
71335-1629-97133516290923 TABLET in 1 BOTTLE (71335-1629-9) 23 tablet1990-01-010000-00-00NoNoCurrent