0173-0569 : Zofran Odt 4 mg Disintegrating Tablet
| NDC: | 0173-0569 |
| Labeler: | Glaxosmithkline LLC |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Zofran Odt |
| Dosage Form: | Oral Tablet, Orally Disintegrating |
| Application #: | NDA020781 |
| Rev. Date: |
Appearance:
| Markings: | Z4 |
| Shapes: |
Round |
| Colors: |
 White |
| Size (mm): | 9 |
| 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. | |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 0173-0569-00: 30 TABLET, ORALLY DISINTEGRATING IN 1 DOSE PACK (0173‑0569‑00)
Active Ingredients:
- Ondansetron
Dosage Strength:
- 4 mg
Inactive Ingredients:
- Aspartame
- Gelatin
- Mannitol
- Methylparaben Sodium
- Propylparaben Sodium
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
- 0173-0489 Zofran 4 mg/5ml Oral Solution 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
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