ondansetron
- Product NDC
- 25021-782
- 11-digit product format
- 250210782
- Labeler code
- 25021
- Product ID
- 25021-782_1513efa2-7d14-40f9-a622-6b69a892e0bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ondansetron hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA090648
- Marketing category
- ANDA
- Marketing start
- 2012-08-30
- Marketing end
- 2021-11-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 25021-782-20 | 25021078220 | 1 VIAL in 1 CARTON (25021-782-20) > 20 mL in 1 VIAL | 1 vial | 2012-08-30 | 2021-11-30 | No | No | Current |