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NDC 00054-0711-28 Deferiprone 1000 mg/1 Details
Deferiprone 1000 mg/1
Deferiprone is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hikma Pharmaceuticals USA Inc.. The primary component is DEFERIPRONE.
MedlinePlus Drug Summary
Deferiprone is used to remove excess iron in the body in adults and children 3 years of age and older who have thalassemia (an inherited condition that causes a low number of red blood cells). It is also used to remove excess iron in adults and children 3 years of age and older with sickle cell disease (an inherited blood disease) or other types of anemia (a lower than normal number of red blood cells). Deferiprone is in a class of medications called iron chelators. It works by attaching to iron in the body so that it can be excreted (removed from the body).
Related Packages: 00054-0711-28Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Deferiprone
Product Information
| NDC | 00054-0711 |
|---|---|
| Product ID | 0054-0711_485546bd-0e6e-46e5-bdbb-02342cae49e2 |
| Associated GPIs | 93100028000340 |
| GCN Sequence Number | 067196 |
| GCN Sequence Number Description | deferiprone TABLET 1000 MG ORAL |
| HIC3 | C8A |
| HIC3 Description | METALLIC POISON,AGENTS TO TREAT |
| GCN | 29687 |
| HICL Sequence Number | 018544 |
| HICL Sequence Number Description | DEFERIPRONE |
| Brand/Generic | Generic |
| Proprietary Name | Deferiprone |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Deferiprone |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, COATED |
| Route | ORAL |
| Active Ingredient Strength | 1000 |
| Active Ingredient Units | mg/1 |
| Substance Name | DEFERIPRONE |
| Labeler Name | Hikma Pharmaceuticals USA Inc. |
| Pharmaceutical Class | Iron Chelating Activity [MoA], Iron Chelator [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA213239 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00054-0711-28 (00054071128)
| NDC Package Code | 0054-0711-28 |
|---|---|
| Billing NDC | 00054071128 |
| Package | 300 TABLET, COATED in 1 BOTTLE (0054-0711-28) |
| Marketing Start Date | 2022-02-08 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |