deferasirox

Product NDC
69238-1702
11-digit product format
692381702
Labeler code
69238
Product ID
69238-1702_30a9b4e3-6d26-43b3-87ba-855df34c9e8d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
deferasirox
Dosage form
GRANULE
Route
ORAL
Labeler
Amneal Pharmaceuticals NY LLC
Application
ANDA214194
Marketing category
ANDA
Marketing start
2021-08-04
Marketing end
0000-00-00
Substance
DEFERASIROX
Active strength
90 mg/1
Pharmacologic classes
Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Iron Chelating Activity [MoA], Iron Chelator [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69238-1702DEFERASIROX GRANULE [AMNEAL PHARMACEUTICALS NY LLC]14Legacy NDC20231230_19f4b412-3d35-4e31-80b6-f13d26c300c5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69238-1702-1692381702011 GRANULE in 1 PACKET (69238-1702-1) 1 granule2021-08-040000-00-00NoNoCurrent
69238-1702-36923817020330 PACKET in 1 CARTON (69238-1702-3) > 1 GRANULE in 1 PACKET (69238-1702-1) 30 packet2021-08-040000-00-00NoNoCurrent