Methylprednisolone

Product NDC
63629-2433
11-digit product format
636292433
Labeler code
63629
Product ID
63629-2433_118f9ee9-cbac-466d-b142-59d88268e48b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methylprednisolone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA040189
Marketing category
ANDA
Marketing start
1997-10-31
Marketing end
0000-00-00
Substance
METHYLPREDNISOLONE
Active strength
4 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
63629-2433-1EA - Each63629-24335b1b3412-4ebe-444f-89f8-79f8882212bd12021-04-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63629-2433METHYLPREDNISOLONE (METHYLPREDNISOLONE) TABLET [BRYANT RANCH PREPACK]103Legacy NDC20240331_232d7d0a-c0c2-4840-9581-f0553e002c4d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-2433-163629243301100 TABLET in 1 BOTTLE (63629-2433-1) 100 tablet2021-02-250000-00-00NoNoCurrent