Ondansetron
- Product NDC
- 68071-4810
- 11-digit product format
- 680714810
- Labeler code
- 68071
- Product ID
- 68071-4810_bb8f3bd6-b405-99e1-e053-2a95a90a8682
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ONDANSETRON
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077548
- Marketing category
- ANDA
- Marketing start
- 2008-10-16
- Marketing end
- 0000-00-00
- Substance
- ONDANSETRON HYDROCHLORIDE
- Active strength
- 2 mg/mL
- 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 |
|---|
| 68071-4810-2 | 68071481002 | 2 mL in 1 VIAL, SINGLE-DOSE (68071-4810-2) | 2 ml | 2019-03-21 | 0000-00-00 | No | No | Current |