67919-041 : Sivextro 200 mg Oral Tablet, Coated

Labeler: Cubist Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Sivextro
Dosage Form: Oral Tablet, Coated
Application #: NDA205435
Rev. Date: 


Markings: TZD;200
Shapes:  Oval
Colors:  Yellow
Size (mm): 14
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:

  • 67919-041-01: 30 TABLET, COATED IN 1 BOTTLE (67919‑041‑01)
  • 67919-041-02: 1 BLISTER PACK IN 1 CARTON (67919‑041‑02) > 6 TABLET, COATED IN 1 BLISTER PACK

Active Ingredients:

  • Tedizolid Phosphate

Dosage Strength:

  • 200 mg

Inactive Ingredients:

  • Cellulose, Microcrystalline
  • Mannitol
  • Crospovidone
  • Povidones
  • Magnesium Stearate
  • Polyvinyl Alcohol
  • Titanium Dioxide
  • Polyethylene Glycols
  • Talc
  • Ferric Oxide Yellow

Pharmaceutical Classes:

  • Oxazolidinone Antibacterial [EPC]
  • Oxazolidinones [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 67919-040 Sivextro 200 mg Intravenous Powder, for Solution by Cubist Pharmaceuticals, Inc.
  • 72000-310 Sivextro 200 mg Oral Tablet, Film Coated by Nabriva Therapeutics Us, Inc.
  • 72000-320 Sivextro 200 mg/4ml Intravenous Injection, Powder, Lyophilized, for Solution by Nabriva Therapeutics Us, Inc.


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Note: The MedsChat® 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.