Ondansetron Hydrochloride
- Product NDC
- 71872-7138
- 11-digit product format
- 718727138
- Labeler code
- 71872
- Product ID
- 71872-7138_9ce5ad2c-3a41-78ff-e053-2995a90a514d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA079224
- Marketing category
- ANDA
- Marketing start
- 2014-12-29
- 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
- 2021-12-31
- 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 |
|---|
| 71872-7138-1 | 71872713801 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7138-1) > 2 mL in 1 VIAL, SINGLE-DOSE | 2018-07-11 | 0000-00-00 | No | No | Current |