Ondansetron Hydrochloride
- Product NDC
- 68151-1668
- 11-digit product format
- 681511668
- Labeler code
- 68151
- Product ID
- 68151-1668_f32643d3-4878-4b78-88c2-1d7334939ed7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA076960
- Marketing category
- ANDA
- Marketing start
- 2006-12-26
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-1668-8 | Ondansetron Hydrochloride | 1 mL in 1 CUP | SOLUTION | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-1668 | ONDANSETRON HYDROCHLORIDE SOLUTION [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20151229_4bfde0e0-09ff-491f-8f57-838ed04ee13c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 68151-1668-8 | 68151166808 | 1 mL in 1 CUP | 1 ml | Historical |