Ondansetron
- Product NDC
- 68071-1904
- 11-digit product format
- 680711904
- Labeler code
- 68071
- Product ID
- 68071-1904_bbf67827-c385-f74d-e053-2a95a90a0693
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA090469
- Marketing category
- ANDA
- Marketing start
- 2010-04-12
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1904-1 | 68071190401 | 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-1904-1) | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1904-2 | 68071190402 | 2 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-1904-2) | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1904-3 | 68071190403 | 3 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-1904-3) | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1904-4 | 68071190404 | 4 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-1904-4) | 2017-02-22 | 0000-00-00 | No | No | Current |
| 68071-1904-6 | 68071190406 | 6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-1904-6) | 2017-02-22 | 0000-00-00 | No | No | Current |