Ondansetron
- Product NDC
- 68071-4911
- 11-digit product format
- 680714911
- Labeler code
- 68071
- Product ID
- 68071-4911_bb9f0d7c-8bdf-e8ef-e053-2a95a90a361a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA091342
- Marketing category
- ANDA
- Marketing start
- 2011-01-27
- Marketing end
- 0000-00-00
- Substance
- ONDANSETRON HYDROCHLORIDE
- Active strength
- 4 mg/5mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4911-5 | 68071491105 | 50 mL in 1 BOTTLE (68071-4911-5) | 50 ml | 2019-05-28 | 0000-00-00 | No | No | Current |