67919-041 : Sivextro 200 mg Oral Tablet, Coated


NDC67919-041
Labeler: Cubist Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Sivextro
Dosage Form: Oral Tablet, Coated
Application #: NDA205435
Rev. Date: 


Appearance:


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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