0143-9597 : Abiraterone 250 mg Oral Tablet
| NDC: | 0143-9597 |
| Labeler: | West-ward Pharmaceuticals Corp |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Abiraterone |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA208339 |
| Rev. Date: |
Appearance:
| Markings: | WW597 |
| Shapes: |
Oval |
| Colors: |
 White |
| Size (mm): | 16 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
NDC Package Codes:
- 0143-9597-21: 120 TABLET IN 1 BOTTLE (0143‑9597‑21)
Active Ingredients:
- Abiraterone Acetate
Dosage Strength:
- 250 mg
Inactive Ingredients:
- Silicon Dioxide
- Croscarmellose Sodium
- Lactose Monohydrate
- Magnesium Stearate
- Cellulose, Microcrystalline
- Povidone
- Sodium Lauryl Sulfate
- Sodium Starch Glycolate Type a Potato /
Pharmaceutical Classes:
- Cytochrome P450 17A1 Inhibitor [EPC]
- Cytochrome P450 17A1 Inhibitors [MoA]
- Cytochrome P450 2C8 Inhibitors [MoA]
- Cytochrome P450 2D6 Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 68001-489 Abiraterone 250 mg Oral Tablet by Bluepoint Laboratories
- 69539-049 Abiraterone 250 mg Oral Tablet by Msn Laboratories Private Limited
- 69539-318 Abiraterone 250 mg Oral Tablet, Film Coated by Msn Laboratories Private Limited
- 69539-319 Abiraterone 500 mg Oral Tablet, Film Coated by Msn Laboratories Private Limited
- 72205-030 Abiraterone 250 mg Oral Tablet by Novadoz Pharmaceuticals LLC
- 72205-284 Abiraterone 250 mg Oral Tablet, Film Coated by Novadoz Pharmaceuticals LLC
- 72205-285 Abiraterone 500 mg Oral Tablet, Film Coated by Novadoz Pharmaceuticals LLC
- 72789-213 Abiraterone 250 mg Oral Tablet by Pd-rx Pharmaceuticals, Inc.
- 82009-139 Abiraterone 250 mg Oral Tablet by Quallent Pharmaceuticals Health LLC
- 82009-140 Abiraterone 500 mg Oral Tablet, Film Coated by Quallent Pharmaceuticals Health LLC
- 82249-010 Abiraterone 250 mg Oral; Oral Tablet by Civicascript, LLC
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.