Ondansetron Hydrochloride
- Product NDC
- 0179-0247
- 11-digit product format
- 001790247
- Labeler code
- 0179
- Product ID
- 0179-0247_7b0cfc48-4ec8-3d28-e053-2991aa0af607
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA078539
- Marketing category
- ANDA
- Marketing start
- 2018-08-30
- Marketing end
- 2020-08-31
- Substance
- ONDANSETRON HYDROCHLORIDE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record