ONDANSETRON
- Product NDC
- 68071-1977
- 11-digit product format
- 680711977
- Labeler code
- 68071
- Product ID
- 68071-1977_62fe2e98-9fe4-2d68-e053-2991aa0ae981
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ONDANSETRON
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record