0173-0442 : Zofran 2 mg/ml Intramuscular; Intravenous Injection


NDC: 0173-0442
Labeler: Glaxosmithkline LLC
Product Type: Human Prescription Drug
Drug Name:  Zofran
Dosage Form: Intramuscular; Intravenous Injection
Application #: NDA020007
Rev. Date: 


NDC Package Codes:

  • 0173-0442-00: 20 ML IN 1 VIAL (0173‑0442‑00)

Active Ingredients:

  • Ondansetron Hydrochloride

Dosage Strength:

  • 2 mg/mL

Pharmaceutical Classes:

  • Serotonin 3 Receptor Antagonists [MoA]
  • Serotonin-3 Receptor Antagonist [EPC]

Related Products:

Based on records with the same trade name.
  • 0173-0446 Zofran 4 mg Oral Tablet by Glaxosmithkline LLC
  • 0173-0447 Zofran (As Ondansetron Hydrochloride Dihydrate) 8 mg Oral Tablet by Glaxosmithkline LLC
  • 0173-0489 Zofran 4 mg/5ml Oral Solution by Glaxosmithkline LLC
  • 0173-0569 Zofran Odt 4 mg Disintegrating Tablet by Glaxosmithkline LLC
  • 0173-0570 Zofran Odt 8 mg Disintegrating Tablet by Glaxosmithkline LLC
  • 0078-0675 Zofran 4 mg Oral Tablet, Film Coated by Novartis Pharmaceuticals Corporation
  • 0078-0676 Zofran 8 mg Oral Tablet, Film Coated by Novartis Pharmaceuticals Corporation
  • 49349-858 Zofran Odt 8 mg Disintegrating Tablet by Remedyrepack Inc.
  • 55154-1132 Zofran 4 mg Oral Tablet by Cardinal Health

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.