Ondansetron
- Product NDC
- 55154-8329
- 11-digit product format
- 551548329
- Labeler code
- 55154
- Product ID
- 55154-8329_7a7fb1ab-8da0-43a2-9054-d0d479e7e070
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Cardinal Health
- Application
- ANDA202600
- Marketing category
- ANDA
- Marketing start
- 2012-12-21
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-8329-5 | 55154832905 | 5 VIAL, SINGLE-DOSE in 1 CARTON (55154-8329-5) > 2 mL in 1 VIAL, SINGLE-DOSE | 2012-12-21 | 0000-00-00 | No | No | Current |