Ondansetron
- Product NDC
- 68071-4566
- 11-digit product format
- 680714566
- Labeler code
- 68071
- Product ID
- 68071-4566_bbefad1f-23b9-5bfd-e053-2a95a90a77f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078152
- Marketing category
- ANDA
- Marketing start
- 2007-06-27
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4566-1 | 68071456601 | 10 TABLET, ORALLY DISINTEGRATING in 1 BOX (68071-4566-1) | 2018-09-18 | 0000-00-00 | No | No | Current |