FERRIPROX

Basic Information

Product Name

FERRIPROX

FDA Product Code

10122-101

Regulatory Information

NDC Product Code

10122-101

Application Number

NDA208030

Marketing Category

C73594

Effective Date

January 5, 2021

Territorial Authority

USA

FDA Title

These highlights do not include all the information needed to use FERRIPROX Oral Solution safely and effectively. See full prescribing information for FERRIPROX Oral Solution.FERRIPROX (deferiprone) oral solution, for oral useInitial U.S. Approval: 2011

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

Active Ingredients

Peppermint Oil

Code: AV092KU4JH

Class Code: IACT

DEFERIPRONE

Quantity: 100 mg in 1 mL

Code: 2BTY8KH53L

Class Code: ACTIB

Water

Code: 059QF0KO0R

Class Code: IACT

Hydroxyethyl Cellulose (2000 Cps At 1%)

Code: S38J6RZN16

Class Code: IACT

Glycerin

Code: PDC6A3C0OX

Class Code: IACT

Hydrochloric Acid

Code: QTT17582CB

Class Code: IACT

Fd&C Yellow No. 6

Code: H77VEI93A8

Class Code: IACT

Sucralose

Code: 96K6UQ3ZD4

Class Code: IACT

Active Moieties

DEFERIPRONE

Code: 2BTY8KH53L

Basic Information

Regulatory Information

Company Information

Active Ingredients

Peppermint Oil

Water

Hydroxyethyl Cellulose (2000 Cps At 1%)

Glycerin

Hydrochloric Acid

Fd&C Yellow No. 6

Sucralose

Active Moieties

DEFERIPRONE