0173-0489 : Zofran 4 mg/5ml Oral Solution


NDC: 0173-0489
Labeler: Glaxosmithkline LLC
Product Type: Human Prescription Drug
Drug Name:  Zofran
Dosage Form: Oral Solution
Application #: NDA020605
Rev. Date: 


NDC Package Codes:

  • 0173-0489-00: 50 ML IN 1 BOTTLE, GLASS (0173‑0489‑00)

Active Ingredients:

  • Ondansetron Hydrochloride

Dosage Strength:

  • 4 mg/5mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0173-0442 Zofran 2 mg/ml Intramuscular; Intravenous Injection by Glaxosmithkline LLC
  • 0173-0446 Zofran 4 mg Oral Tablet by Glaxosmithkline LLC
  • 0173-0447 Zofran (As Ondansetron Hydrochloride Dihydrate) 8 mg Oral Tablet by Glaxosmithkline LLC
  • 0173-0569 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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NDC 0173-0489 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.