Ondansetron
- Product NDC
- 60687-636
- 11-digit product format
- 606870636
- Labeler code
- 60687
- Product ID
- 60687-636_e5c40965-650a-3b04-e053-2a95a90a8daa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA077851
- Marketing category
- ANDA
- Marketing start
- 2022-08-20
- 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
- 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 |
|---|
| 60687-636-01 | 60687063601 | 100 BLISTER PACK in 1 CARTON (60687-636-01) > 1 TABLET in 1 BLISTER PACK (60687-636-11) | 100 blister pack | 2022-08-20 | 0000-00-00 | No | No | Current |