59212-111 : Nilandron 150 mg Oral Tablet
NDC: | 59212-111 |
Labeler: | Concordia Pharmaceuticals Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Nilandron |
Dosage Form: | Oral Tablet |
Application #: | NDA020169 |
Rev. Date: |
Appearance:
Markings: | 168D |
Shapes: |
Round |
Colors: |
White |
Size (mm): | 10 |
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. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 59212-111-10: 1 BLISTER PACK IN 1 CARTON (59212‑111‑10) > 10 TABLET IN 1 BLISTER PACK
- 59212-111-14: 1 BLISTER PACK IN 1 CARTON (59212‑111‑14) > 30 TABLET IN 1 BLISTER PACK
Active Ingredients:
- Nilutamide
Dosage Strength:
- 150 mg
Inactive Ingredients:
- Starch, Corn
- Lactose
- Povidones
- Docusate Sodium
- Magnesium Stearate
- Talc
Pharmaceutical Classes:
- Androgen Receptor Antagonists [MoA]
- Androgen Receptor Inhibitor [EPC]
Related Products:
Based on records with the same trade name.- 0088-1111 Nilandron 150 mg Oral Tablet by Sanofi-aventis U.S. LLC
- 24987-111 Nilandron 150 mg Oral Tablet by Covis Pharmaceuticals, 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.