Ondansetron
- Product NDC
- 71930-018
- 11-digit product format
- 719300018
- Labeler code
- 71930
- Product ID
- 71930-018_13d17c94-b480-4c55-b45a-0302e9d6a6cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Eywa Pharma Inc.
- Application
- ANDA077851
- Marketing category
- ANDA
- Marketing start
- 2018-07-11
- Marketing end
- 0000-00-00
- Substance
- ONDANSETRON HYDROCHLORIDE
- Active strength
- 8 mg/1
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71930-018-30 | 71930001830 | 30 TABLET in 1 BOTTLE (71930-018-30) | 30 tablet | 2018-07-11 | 0000-00-00 | No | No | Current |
| 71930-018-52 | 71930001852 | 500 TABLET in 1 BOTTLE (71930-018-52) | 500 tablet | 2020-02-06 | 0000-00-00 | No | No | Current |