PredniSONE

Product NDC
71335-1220
11-digit product format
713351220
Labeler code
71335
Product ID
71335-1220_5d5155f3-cf29-4b14-a8fa-a7c73643dea9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PredniSONE
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA080352
Marketing category
ANDA
Marketing start
1972-04-21
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-1220-4EA - Each71335-1220ded99716-3c78-49d4-bd9d-c8e54f39dc7212020-04-20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1220-07133512200042 TABLET in 1 BOTTLE (71335-1220-0) 42 tablet2021-12-280000-00-00NoNoCurrent
71335-1220-17133512200130 TABLET in 1 BOTTLE (71335-1220-1) 30 tablet2019-05-090000-00-00NoNoCurrent
71335-1220-27133512200278 TABLET in 1 BOTTLE (71335-1220-2) 78 tablet2021-12-280000-00-00NoNoCurrent
71335-1220-37133512200336 TABLET in 1 BOTTLE (71335-1220-3) 36 tablet2021-12-280000-00-00NoNoCurrent
71335-1220-47133512200421 TABLET in 1 BOTTLE (71335-1220-4) 21 tablet2019-05-300000-00-00NoNoCurrent
71335-1220-57133512200515 TABLET in 1 BOTTLE (71335-1220-5) 15 tablet2021-12-280000-00-00NoNoCurrent
71335-1220-671335122006100 TABLET in 1 BOTTLE (71335-1220-6) 100 tablet2019-07-120000-00-00NoNoCurrent
71335-1220-77133512200720 TABLET in 1 BOTTLE (71335-1220-7) 20 tablet2019-12-030000-00-00NoNoCurrent
71335-1220-87133512200810 TABLET in 1 BOTTLE (71335-1220-8) 10 tablet2019-05-090000-00-00NoNoCurrent
71335-1220-97133512200990 TABLET in 1 BOTTLE (71335-1220-9) 90 tablet2021-12-280000-00-00NoNoCurrent