Ondansetron
- Product NDC
- 55700-672
- 11-digit product format
- 557000672
- Labeler code
- 55700
- Product ID
- 55700-672_edbada61-430f-49c9-8774-067dab043903
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA090469
- Marketing category
- ANDA
- Marketing start
- 2018-08-24
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-672-10 | 55700067210 | 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (55700-672-10) | 2018-08-24 | 0000-00-00 | No | No | Current |
| 55700-672-65 | 55700067265 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (55700-672-65) | 2018-09-14 | 0000-00-00 | No | No | Current |