Ondansetron
- Product NDC
- 0904-7073
- 11-digit product format
- 009047073
- Labeler code
- 0904
- Product ID
- 0904-7073_fa2e1ce8-e4c2-4b85-bdc8-532ad510d5b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA091483
- Marketing category
- ANDA
- Marketing start
- 2010-12-17
- 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
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7073 | ONDANSETRON SOLUTION [MAJOR PHARMACEUTICALS] | 6 | Legacy NDC | 20250402_3e3677bb-9b43-4c93-b65b-7491f4019e24.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7073-93 | 00904707393 | 30 CUP in 1 CARTON (0904-7073-93) > 5 mL in 1 CUP (0904-7073-41) | 30 cup | 2010-12-17 | 0000-00-00 | No | No | Current |