PREDNISONE

Product NDC
71335-1915
11-digit product format
713351915
Labeler code
71335
Product ID
71335-1915_496b156e-d3fd-4a01-8c47-e782e40bb8a4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prednisone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA210525
Marketing category
ANDA
Marketing start
2018-12-04
Marketing end
0000-00-00
Substance
PREDNISONE
Active strength
10 mg/1
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1915-07133519150010 TABLET in 1 BOTTLE, PLASTIC (71335-1915-0) 10 tablet2021-07-200000-00-00NoNoCurrent
71335-1915-17133519150121 TABLET in 1 BOTTLE, PLASTIC (71335-1915-1) 21 tablet2021-07-200000-00-00NoNoCurrent
71335-1915-27133519150240 TABLET in 1 BOTTLE, PLASTIC (71335-1915-2) 40 tablet2021-07-200000-00-00NoNoCurrent
71335-1915-37133519150330 TABLET in 1 BOTTLE, PLASTIC (71335-1915-3) 30 tablet2021-07-200000-00-00NoNoCurrent
71335-1915-47133519150420 TABLET in 1 BOTTLE, PLASTIC (71335-1915-4) 20 tablet2021-07-200000-00-00NoNoCurrent
71335-1915-57133519150515 TABLET in 1 BOTTLE, PLASTIC (71335-1915-5) 15 tablet2021-07-200000-00-00NoNoCurrent
71335-1915-67133519150650 TABLET in 1 BOTTLE, PLASTIC (71335-1915-6) 50 tablet2021-07-200000-00-00NoNoCurrent
71335-1915-77133519150760 TABLET in 1 BOTTLE, PLASTIC (71335-1915-7) 60 tablet2021-07-200000-00-00NoNoCurrent
71335-1915-87133519150842 TABLET in 1 BOTTLE, PLASTIC (71335-1915-8) 42 tablet2021-07-200000-00-00NoNoCurrent
71335-1915-97133519150948 TABLET in 1 BOTTLE, PLASTIC (71335-1915-9) 48 tablet2021-07-200000-00-00NoNoCurrent