MethylPREDNISolone

Product NDC
63739-133
11-digit product format
637390133
Labeler code
63739
Product ID
63739-133_2d1b064c-c50f-4168-b66b-f956795d18e8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
methylprednisolone
Dosage form
TABLET
Route
ORAL
Labeler
McKesson Corporation dba SKY Packaging
Application
ANDA040183
Marketing category
ANDA
Marketing start
1998-12-22
Marketing end
0000-00-00
Substance
METHYLPREDNISOLONE
Active strength
4 mg/1
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63739-133-102020-07-22C16284748780-1ab0e2407-272f-f274-e053-dbdaa90a647156718982-4ccf-47a4-8052-ac7de45e13a8

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63739-133-10EA - Each63739-13354c539ed-54b9-46b2-8560-3a556675ee6b12017-03-06