Ondansetron Hydrochloride
- Product NDC
- 23155-168
- 11-digit product format
- 231550168
- Labeler code
- 23155
- Product ID
- 23155-168_ad6dc125-1b99-4e50-ac4f-eca143164f41
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Heritage Pharmaceuticals Inc.
- Application
- ANDA090424
- Marketing category
- ANDA
- Marketing start
- 2012-12-13
- Marketing end
- 0000-00-00
- Substance
- ONDANSETRON HYDROCHLORIDE
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record