PREDNISOLONE SODIUM PHOSPHATE

Product NDC
13985-025
11-digit product format
139850025
Labeler code
13985
Product ID
13985-025_dbcab023-8a71-4c66-ac6b-b98b20a493f9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PREDNISOLONE SODIUM PHOSPHATE
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
MWI/VetOne
Application
ANDA040070
Marketing category
ANDA
Marketing start
1994-07-29
Marketing end
0000-00-00
Substance
PREDNISOLONE SODIUM PHOSPHATE
Active strength
10 mg/mL
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
13985-025-022024-10-28C16284748780-1960f7f55-d05b-8e05-e053-dbdaa90a074adbcab023-8a71-4c66-ac6b-b98b20a493f9
13985-025-022019-10-29C16284748780-1960f7f55-d05b-8e05-e053-dbdaa90a074adbcab023-8a71-4c66-ac6b-b98b20a493f9