PREDNISONE

Product NDC
71335-1628
11-digit product format
713351628
Labeler code
71335
Product ID
71335-1628_0b7e061a-26aa-4a77-bdac-a4890f3043bf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prednisone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA211495
Marketing category
ANDA
Marketing start
2018-12-07
Marketing end
0000-00-00
Substance
PREDNISONE
Active strength
5 mg/1
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1628-07133516280042 TABLET in 1 BOTTLE (71335-1628-0) 42 tablet2022-01-280000-00-00NoNoCurrent
71335-1628-17133516280130 TABLET in 1 BOTTLE (71335-1628-1) 30 tablet2022-01-280000-00-00NoNoCurrent
71335-1628-27133516280278 TABLET in 1 BOTTLE (71335-1628-2) 78 tablet2022-01-280000-00-00NoNoCurrent
71335-1628-37133516280336 TABLET in 1 BOTTLE (71335-1628-3) 36 tablet2022-01-280000-00-00NoNoCurrent
71335-1628-47133516280421 TABLET in 1 BOTTLE (71335-1628-4) 21 tablet2022-01-280000-00-00NoNoCurrent
71335-1628-57133516280515 TABLET in 1 BOTTLE (71335-1628-5) 15 tablet2022-01-280000-00-00NoNoCurrent
71335-1628-671335162806100 TABLET in 1 BOTTLE (71335-1628-6) 100 tablet2022-01-280000-00-00NoNoCurrent
71335-1628-77133516280720 TABLET in 1 BOTTLE (71335-1628-7) 20 tablet2022-01-280000-00-00NoNoCurrent
71335-1628-87133516280810 TABLET in 1 BOTTLE (71335-1628-8) 10 tablet2022-01-280000-00-00NoNoCurrent
71335-1628-97133516280990 TABLET in 1 BOTTLE (71335-1628-9) 90 tablet2022-01-280000-00-00NoNoCurrent