Ondansetron
- Product NDC
- 68788-9329
- 11-digit product format
- 687889329
- Labeler code
- 68788
- Product ID
- 68788-9329_60287879-48cd-47da-8560-3ea12c9a6312
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078152
- Marketing category
- ANDA
- Marketing start
- 2015-03-31
- 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