51672-4196 : Deferiprone 500 mg Oral Tablet
| NDC: | 51672-4196 |
| Labeler: | Taro Pharmaceuticals U.S.a., Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Deferiprone |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA208800 |
| Rev. Date: |
Appearance:
| Markings: | T;5 |
| Shapes: |
Oval |
| Colors: |
 White |
| Size (mm): | 18 |
| Segments: * | 2 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces. | |
NDC Package Codes:
- 51672-4196-1: 100 TABLET IN 1 BOTTLE (51672‑4196‑1)
Active Ingredients:
- Deferiprone
Dosage Strength:
- 500 mg
Inactive Ingredients:
- Microcrystalline Cellulose
- Silicon Dioxide
- Magnesium Stearate /
Pharmaceutical Classes:
- Iron Chelating Activity [MoA]
- Iron Chelator [EPC]
Related Products:
Based on records with the same trade name.- 51672-4237 Deferiprone 1000 mg Oral Tablet by Taro Pharmaceuticals U.S.a., Inc.
- 0054-0576 Deferiprone 500 mg Oral Tablet, Coated by Hikma Pharmaceuticals USA Inc.
- 0054-0711 Deferiprone 1000 mg Oral Tablet, Coated by Hikma Pharmaceuticals USA Inc.
NDC QR Code
Scan the QR code below to easily reference this data in the future:
< Prev: 51672-4194Next: 51672-4197 >
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.