0054-0711 : Deferiprone 1000 mg Oral Tablet, Coated
NDC: | 0054-0711 |
Labeler: | Hikma Pharmaceuticals USA Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | ![]() |
Dosage Form: | Oral Tablet, Coated |
Application #: | ANDA213239 |
Rev. Date: |
NDC Package Codes:
- 0054-0711-19: 50 TABLET, COATED IN 1 BOTTLE (0054‑0711‑19)
- 0054-0711-23: 150 TABLET, COATED IN 1 BOTTLE (0054‑0711‑23)
- 0054-0711-28: 300 TABLET, COATED IN 1 BOTTLE (0054‑0711‑28)
Active Ingredients:
- Deferiprone
Dosage Strength:
- 1000 mg
Pharmaceutical Classes:
- Iron Chelating Activity [MoA]
- Iron Chelator [EPC]
Related Products:
Based on records with the same trade name.- 0054-0576 Deferiprone 500 mg Oral Tablet, Coated by Hikma Pharmaceuticals USA Inc.
- 51672-4196 Deferiprone 500 mg Oral Tablet by Taro Pharmaceuticals U.S.a., Inc.
- 51672-4237 Deferiprone 1000 mg Oral Tablet by Taro Pharmaceuticals U.S.a., Inc.
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.