Ondansetron
- Product NDC
- 55154-2876
- 11-digit product format
- 551542876
- Labeler code
- 55154
- Product ID
- 55154-2876_5f4e1ec0-a5ac-4196-9df2-86de29a55533
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA077541
- Marketing category
- ANDA
- Marketing start
- 2006-12-26
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ondansetron
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ONDANSETRON HYDROCHLORIDE | 2 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | NMH84OZK2B |
| Rxcui | 1740467 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55154-2876 | ONDANSETRON INJECTION [CARDINAL HEALTH 107, LLC] | 188557109 | Current NDC, Legacy NDC, 2 package rows | 20240319_ee1f115f-c8f8-4526-b827-c8e48aeb5050.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-2876-5 | 55154287605 | 5 VIAL in 1 BAG (55154-2876-5) / 2 mL in 1 VIAL | 5 vial | 2006-12-26 | 0000-00-00 | No | No | Current |