Prednisone

Product NDC
71335-0857
11-digit product format
713350857
Labeler code
71335
Product ID
71335-0857_7ac5d1c3-3bd8-4ae3-b95c-57934ea3c11e
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
71335-0857-07133508570011 TABLET in 1 BOTTLE (71335-0857-0) 11 tablet2013-01-220000-00-00NoNoCurrent
71335-0857-17133508570120 TABLET in 1 BOTTLE (71335-0857-1) 20 tablet2013-01-220000-00-00NoNoCurrent
71335-0857-27133508570230 TABLET in 1 BOTTLE (71335-0857-2) 30 tablet2013-01-220000-00-00NoNoCurrent
71335-0857-37133508570340 TABLET in 1 BOTTLE (71335-0857-3) 40 tablet2013-01-220000-00-00NoNoCurrent
71335-0857-47133508570415 TABLET in 1 BOTTLE (71335-0857-4) 15 tablet2013-01-220000-00-00NoNoCurrent
71335-0857-57133508570510 TABLET in 1 BOTTLE (71335-0857-5) 10 tablet2013-01-220000-00-00NoNoCurrent
71335-0857-67133508570621 TABLET in 1 BOTTLE (71335-0857-6) 21 tablet2013-01-220000-00-00NoNoCurrent
71335-0857-77133508570718 TABLET in 1 BOTTLE (71335-0857-7) 18 tablet2013-01-220000-00-00NoNoCurrent
71335-0857-87133508570812 TABLET in 1 BOTTLE (71335-0857-8) 12 tablet2013-01-220000-00-00NoNoCurrent
71335-0857-97133508570923 TABLET in 1 BOTTLE (71335-0857-9) 23 tablet2013-01-220000-00-00NoNoCurrent