NDC 10122-100

FERRIPROX

Deferiprone

FERRIPROX is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Chiesi Usa, Inc.. The primary component is Deferiprone.

Product ID10122-100_7c82e2f1-fe2d-4412-8d12-e5da5cedb9e9
NDC10122-100
Product TypeHuman Prescription Drug
Proprietary NameFERRIPROX
Generic NameDeferiprone
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2011-11-25
Marketing CategoryNDA / NDA
Application NumberNDA021825
Labeler NameChiesi USA, Inc.
Substance NameDEFERIPRONE
Active Ingredient Strength500 mg/1
Pharm ClassesIron Chelating Activity [MoA],Iron Chelator [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 10122-100-10

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10122-100-10)
Marketing Start Date2021-01-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "FERRIPROX" or generic name "Deferiprone"

NDCBrand NameGeneric Name
10122-100FERRIPROXdeferiprone
10122-101FERRIPROXdeferiprone
10122-103FERRIPROXDEFERIPRONE
10122-104FERRIPROXdeferiprone
52609-0006FERRIPROXdeferiprone
52609-0007FERRIPROXdeferiprone
52609-4502FERRIPROXdeferiprone
0054-0576DeferiproneDeferiprone
0054-0711DeferiproneDeferiprone
51672-4196DeferiproneDeferiprone

Trademark Results [FERRIPROX]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FERRIPROX
FERRIPROX
75719191 2550510 Live/Registered
APOTEX INC.
1999-05-28

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