0078-0415 : Zortress 0.75 mg Oral Tablet
NDC: | 0078-0415 |
Labeler: | Novartis Pharmaceuticals Corporation |
Product Type: | Human Prescription Drug |
Drug Name: | Zortress |
Dosage Form: | Oral Tablet |
Application #: | NDA021560 |
Rev. Date: |
Appearance:
Markings: | CL;NVR |
Shapes: |
Round |
Colors: |
White |
Size (mm): | 9 |
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:
- 0078-0415-20: 60 BLISTER PACK IN 1 BOX (0078‑0415‑20) > 1 TABLET IN 1 BLISTER PACK (0078‑0415‑61)
Active Ingredients:
- Everolimus
Dosage Strength:
- .75 mg
Inactive Ingredients:
- Butylated Hydroxytoluene
- Crospovidone
- Hypromelloses
- Anhydrous Lactose
- Lactose Monohydrate
- Magnesium Stearate
Pharmaceutical Classes:
- Kinase Inhibitor [EPC]
- Protein Kinase Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 0078-0414 Zortress 0.5 mg Oral Tablet by Novartis Pharmaceuticals Corporation
- 0078-0417 Zortress 0.25 mg Oral Tablet by Novartis Pharmaceuticals Corporation
- 0078-0422 Zortress 1 mg Oral Tablet by Novartis Pharmaceuticals Corporation
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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.