Ondansetron Hydrochloride
- Product NDC
- 55154-8176
- 11-digit product format
- 551548176
- Labeler code
- 55154
- Product ID
- 55154-8176_3af2981f-e9f9-4ccd-815a-9a9f05c47f49
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA078539
- Marketing category
- ANDA
- Marketing start
- 2012-07-16
- Marketing end
- 2024-04-30
- Substance
- ONDANSETRON HYDROCHLORIDE
- Active strength
- 4 mg/1
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| NMH84OZK2B | ONDANSETRON HYDROCHLORIDE | 103639-04-9 | ONDANSETRON HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-8176-0 | 55154817600 | 10 BLISTER PACK in 1 BAG (55154-8176-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2012-07-16 | 2024-04-30 | No | No | Current |