ondansetron
- Product NDC
- 68788-7705
- 11-digit product format
- 687887705
- Labeler code
- 68788
- Product ID
- 68788-7705_aa7e55f3-0032-49f5-b687-13176abfa934
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA077557
- Marketing category
- ANDA
- Marketing start
- 2020-05-01
- Marketing end
- 0000-00-00
- Substance
- ONDANSETRON
- Active strength
- 8 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7705-1 | 68788770501 | 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68788-7705-1) | 2020-05-01 | 0000-00-00 | No | No | Current |
| 68788-7705-3 | 68788770503 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68788-7705-3) | 2020-05-01 | 0000-00-00 | No | No | Current |