Ondansetron Hydrochloride
- Product NDC
- 50436-0187
- 11-digit product format
- 504360187
- Labeler code
- 50436
- Product ID
- 50436-0187_1fbdf71c-6410-4a60-98b2-05e857587bad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA078539
- Marketing category
- ANDA
- Marketing start
- 2007-07-31
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- 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 |
|---|
| 50436-0187-1 | Ondansetron Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 6 |
| 50436-0187-4 | Ondansetron Hydrochloride | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0187 | ONDANSETRON HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 6 | Legacy NDC, 2 package rows | 20210905_0309ecf4-bb8e-439a-9c15-f749f50576bb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50436-0187-1 | 50436018701 | 30 TABLET, FILM COATED in 1 BOTTLE (50436-0187-1) | 2016-07-04 | 0000-00-00 | No | No | Current |
| 50436-0187-4 | 50436018704 | 10 TABLET, FILM COATED in 1 BOTTLE (50436-0187-4) | 2016-07-04 | 0000-00-00 | No | No | Current |