0078-0422 : Zortress 1 mg Oral Tablet


NDC: 0078-0422
Labeler: Novartis Pharmaceuticals Corporation
Product Type: Human Prescription Drug
Drug Name:  Zortress
Dosage Form: Oral Tablet
Application #: NDA021560
Rev. Date: 


Appearance:


Markings: CU;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:

  • 0078-0422-20: 60 BLISTER PACK IN 1 BOX (0078‑0422‑20) > 1 TABLET IN 1 BLISTER PACK (0078‑0422‑61)

Active Ingredients:

  • Everolimus

Dosage Strength:

  • 1 mg

Inactive Ingredients:

  • Butylated Hydroxytoluene
  • Crospovidone
  • Hypromelloses
  • Anhydrous Lactose
  • Lactose Monohydrate
  • Magnesium Stearate /

Pharmaceutical Classes:

  • Kinase Inhibitor [EPC]
  • Protein Kinase Inhibitors [MoA]
  • Cytochrome P450 3A4 Inhibitors [MoA]
  • P-Glycoprotein Inhibitors [MoA]
  • Cytochrome P450 2D6 Inhibitors [MoA]
  • mTOR Inhibitor Immunosuppressant [EPC]
  • mTOR Inhibitors [MoA]
  • Decreased Immunologic Activity [PE]

Related Products:

Based on records with the same trade name.
  • 0078-0414 Zortress 0.5 mg Oral Tablet by Novartis Pharmaceuticals Corporation
  • 0078-0415 Zortress 0.75 mg Oral Tablet by Novartis Pharmaceuticals Corporation
  • 0078-0417 Zortress 0.25 mg Oral Tablet by Novartis Pharmaceuticals Corporation

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.