Ondansetron
- Product NDC
- 55154-5431
- 11-digit product format
- 551545431
- Labeler code
- 55154
- Product ID
- 55154-5431_66fcdc82-fede-45b4-b14a-3e77ca948ae4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA078050
- Marketing category
- ANDA
- Marketing start
- 2007-08-31
- Marketing end
- 0000-00-00
- Substance
- ONDANSETRON
- Active strength
- 4 mg/1
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record