Ondansetron
- Product NDC
- 70518-0828
- 11-digit product format
- 705180828
- Labeler code
- 70518
- Product ID
- 70518-0828_8edc21f1-1656-bd92-e053-2995a90aed02
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078050
- Marketing category
- ANDA
- Marketing start
- 2017-11-08
- Marketing end
- 0000-00-00
- Substance
- ONDANSETRON
- Active strength
- 8 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