Ondansetron
- Product NDC
- 68071-1658
- 11-digit product format
- 680711658
- Labeler code
- 68071
- Product ID
- 68071-1658_592cd7cb-bde7-906b-e053-2a91aa0a917d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078050
- Marketing category
- ANDA
- Marketing start
- 2007-08-13
- 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