ZOFRAN
- Product NDC
- 0078-0676
- 11-digit product format
- 000780676
- Labeler code
- 0078
- Product ID
- 0078-0676_8d673085-eea1-4bd0-8804-a6cc63038973
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ondansetron hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Novartis Pharmaceuticals Corporation
- Application
- NDA020103
- Marketing category
- NDA
- Marketing start
- 2017-12-12
- Marketing end
- 2022-05-31
- 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
- 0000-00-00
- 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 |
|---|
| 0078-0676-15 | 00078067615 | 30 TABLET, FILM COATED in 1 BOTTLE (0078-0676-15) | 2017-12-12 | 0000-00-00 | No | No | Current |