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FERRIPROX
FERRIPROX - 52609-0006-1 - (deferiprone)
Drug Information of FERRIPROX
| Product NDC: | 52609-0006 |
| Proprietary Name: | FERRIPROX |
| Non Proprietary Name: | deferiprone |
| Active Ingredient(s): | 500 mg/1 & nbsp; deferiprone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FERRIPROX
| Product NDC: | 52609-0006 |
| Labeler Name: | ApoPharma USA, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021825 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20111125 |
Package Information of FERRIPROX
| Package NDC: | 52609-0006-1 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52609-0006-1) |
NDC Information of FERRIPROX
| NDC Code | 52609-0006-1 |
| Proprietary Name | FERRIPROX |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52609-0006-1) |
| Product NDC | 52609-0006 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | deferiprone |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111125 |
| Marketing Category Name | NDA |
| Labeler Name | ApoPharma USA, Inc. |
| Substance Name | DEFERIPRONE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Iron Chelating Activity [MoA],Iron Chelator [EPC] |
