Deferasirox

Product NDC
43598-852
11-digit product format
435980852
Labeler code
43598
Product ID
43598-852_95a20658-492c-6693-491b-f651f3a2f25f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Deferasirox
Dosage form
TABLET
Route
ORAL
Labeler
Dr. Reddy's Laboratories Inc
Application
ANDA210945
Marketing category
ANDA
Marketing start
2020-06-25
Substance
DEFERASIROX
Active strength
180 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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
V8G4MOF2V9DEFERASIROX201530-41-8DEFERASIROX

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
43598-852-10435980852101000 TABLET in 1 BOTTLE (43598-852-10) 1000 tablet2020-06-25NoNoHistorical
43598-852-304359808523030 TABLET in 1 BOTTLE (43598-852-30) 30 tablet2020-06-25NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
DeferasiroxDr. Reddy's Laboratories Inc | MSN LABORATORIES PRIVATE LIMITED2024-09-30HUMAN PRESCRIPTION DRUG LABEL5