Ondansetron Hydrochloride
- Product NDC
- 23155-196
- 11-digit product format
- 231550196
- Labeler code
- 23155
- Product ID
- 23155-196_0b9de743-fe73-47e4-ab1f-a88cb1392ce6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Heritage Pharmaceuticals Inc.
- Application
- ANDA078945
- Marketing category
- ANDA
- Marketing start
- 2013-01-18
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 23155-196-41 | 23155019641 | 5 VIAL in 1 CARTON (23155-196-41) > 2 mL in 1 VIAL (23155-196-31) | 5 vial | 2013-01-18 | 0000-00-00 | No | No | Current |
| 23155-196-42 | 23155019642 | 10 VIAL in 1 CARTON (23155-196-42) > 2 mL in 1 VIAL (23155-196-31) | 10 vial | 2013-01-18 | 0000-00-00 | No | No | Current |
| 23155-196-43 | 23155019643 | 25 VIAL in 1 CARTON (23155-196-43) > 2 mL in 1 VIAL (23155-196-31) | 25 vial | 2013-01-18 | 0000-00-00 | No | No | Current |