Prednisolone Sodium Phosphate

Product NDC
60432-212
11-digit product format
604320212
Labeler code
60432
Product ID
60432-212_c1ac7268-6f03-4c8b-ab36-d8695aa56e67
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prednisolone Sodium Phosphate
Dosage form
SOLUTION
Route
ORAL
Labeler
Morton Grove Pharmaceuticals, Inc.
Application
ANDA076895
Marketing category
ANDA
Marketing start
2004-10-04
Marketing end
0000-00-00
Substance
PREDNISOLONE SODIUM PHOSPHATE
Active strength
15 mg/5mL
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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b3fecff3-fb51-4f66-b443-a130905bb500Product name120250804
3a7a0034-a88d-88c3-f43e-ea34c6a216deProduct name220250311
9dbc4744-f7be-4393-b71a-e1bfd8b97659Product name220250218
9e44d9f9-cb87-3b0f-4c71-c8438d0dc2e5Product name220240102
a0e37fa3-7f16-4fbf-bdb7-ae82cb1a553aProduct name120170309
af7d3306-1338-423f-839e-419aad9e8a86Product name120170309
18d57d04-4a34-a130-5dd5-b7fc47f3b567Product name120140508
379bc253-901a-e6e1-92b7-0fc574249e07Product name120140508
48b05f5d-d2fc-45ab-76e8-3cb5bd44890dProduct name120140508
73adedd8-aba8-27d9-78d9-2e3c4a3cf954Product name120140508
9ae74339-0a3d-82e9-5dd1-88bd2607bd6bProduct name120140508
9f10552a-9a7b-8e6c-3223-dc44310af6cfProduct name120140508
e44e38a9-2d9e-b0e2-cce9-490554639f3dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60432-212-082025-12-12C16284748780-1f386c649-ae70-0266-e053-dadaa90a7c1a9f4b181e-2675-40c6-a3d7-a8fe671230c1
60432-212-082023-01-30C16284748780-1f386c649-ae70-0266-e053-dadaa90a7c1a9f4b181e-2675-40c6-a3d7-a8fe671230c1

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60432-212-08ML - Milliliter60432-2120ee5ddf0-441d-4149-911a-489c5762ca5912012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60432-212PREDNISOLONE SODIUM PHOSPHATE SOLUTION [MORTON GROVE PHARMACEUTICALS, INC.]6Legacy NDC20210924_9f4b181e-2675-40c6-a3d7-a8fe671230c1.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
283077prednisoLONE sodium phosphate 15 MG in 5 mL Oral SolutionPSNdfbab230-113f-4da7-94f0-76111c681d327
283077prednisolone 3 MG/ML Oral SolutionSCDdfbab230-113f-4da7-94f0-76111c681d327
283077prednisolone 15 MG (as prednisolone sodium phosphate 20.2 MG) per 5 ML Oral SolutionSYdfbab230-113f-4da7-94f0-76111c681d327
283077prednisolone 15 MG per 5 ML Oral SolutionSYdfbab230-113f-4da7-94f0-76111c681d327

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60432-212-0860432021208237 mL in 1 BOTTLE, PLASTIC (60432-212-08) 237 ml2004-10-040000-00-00NoNoCurrent