Ondansetron
- Product NDC
- 50436-0134
- 11-digit product format
- 504360134
- Labeler code
- 50436
- Product ID
- 50436-0134_83aa2360-ad96-400f-88f9-80208901b89e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA078152
- Marketing category
- ANDA
- Marketing start
- 2007-06-27
- Marketing end
- 0000-00-00
- Substance
- ONDANSETRON
- Active strength
- 4 mg/1
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50436-0134-1 | Ondansetron | 10 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 10 | | 3 |
| 50436-0134-1 | Ondansetron | 3 in 1 BOX, UNIT-DOSE | TABLET, ORALLY DISINTEGRATING | 3 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0134 | ONDANSETRON TABLET, ORALLY DISINTEGRATING [UNIT DOSE SERVICES] | 3 | Legacy NDC, 2 package rows | 20170711_92a8467d-aece-45ae-b8c8-21988901ba5f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0134-1 | 50436013401 | 10 in 1 BLISTER PACK | Historical |