Ondansetron
- Product NDC
- 68071-1649
- 11-digit product format
- 680711649
- Labeler code
- 68071
- Product ID
- 68071-1649_bb1249d2-2290-c949-e053-2995a90add80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ondansetron hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077009
- Marketing category
- ANDA
- Marketing start
- 2007-11-30
- 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 |
|---|
| 68071-1649-5 | 68071164905 | 50 mL in 1 BOTTLE (68071-1649-5) | 50 ml | 2018-09-24 | 0000-00-00 | No | No | Current |