67919-040 : Sivextro 200 mg Intravenous Powder, for Solution


NDC67919-040
Labeler: Cubist Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Sivextro
Dosage Form: Intravenous Powder, for Solution
Application #: NDA205436
Rev. Date: 


NDC Package Codes:

  • 67919-040-01: 10 VIAL, GLASS IN 1 CARTON (67919‑040‑01) > 1 POWDER, FOR SOLUTION IN 1 VIAL, GLASS
  • 67919-040-02: 10 VIAL, GLASS IN 1 CARTON (67919‑040‑02) / 4 ML IN 1 VIAL, GLASS

Active Ingredients:

  • Tedizolid Phosphate

Dosage Strength:

  • 200 mg/4mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 67919-041 Sivextro 200 mg Oral Tablet, Coated 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.

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.