ondansetron
- Product NDC
- 50090-2104
- 11-digit product format
- 500902104
- Labeler code
- 50090
- Product ID
- 50090-2104_66525751-71c6-4e31-89ef-c11dd4217ac9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077557
- Marketing category
- ANDA
- Marketing start
- 2007-08-02
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record