Sun Pharmaceutical Industries Limited
Halol, India · makes it and tests it
Serious problems, FDA action Last FDA inspection Jun 13, 2025. 12 inspections on record, 5 with serious problems.
NDC 50436-0131
ondansetron hydrochloride 8 mg tablet, film coated
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 62756-131.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Product details
- Generic drug
- Ondansetron: see every company that makes it
- Form
- tablet, film coated
- Strength
- 8 mg
- Approval
- ANDA ANDA077050
- On the market since
- Jun 25, 2007
- Package NDCs
50436-0131-1- Official label
- DailyMed (National Library of Medicine), updated Feb 27, 2017
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