PredniSONE

Product NDC
70934-137
11-digit product format
709340137
Labeler code
70934
Product ID
70934-137_b9bbdd9b-42c8-69d1-e053-2a95a90a35d6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PredniSONE
Dosage form
TABLET
Route
ORAL
Labeler
Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Application
ANDA084283
Marketing category
ANDA
Marketing start
2018-06-20
Marketing end
0000-00-00
Substance
PREDNISONE
Active strength
50 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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70934-137-05EA - Each70934-1373aa7597e-082d-4557-ba24-3a8c990d2eb712018-09-05

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70934-137-05709340137055 TABLET in 1 BOTTLE, PLASTIC (70934-137-05) 5 tablet2018-06-200000-00-00NoNoCurrent
70934-137-07709340137077 TABLET in 1 BOTTLE, PLASTIC (70934-137-07) 7 tablet2019-06-270000-00-00NoNoCurrent