Ondansetron
- Product NDC
- 63629-7513
- 11-digit product format
- 636297513
- Labeler code
- 63629
- Product ID
- 63629-7513_f243b55b-00a0-4dbb-aec3-8623d4e31cde
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record