ondansetron hydrochloride
- Product NDC
- 68788-9892
- 11-digit product format
- 687889892
- Labeler code
- 68788
- Product ID
- 68788-9892_c4efe126-6f10-4a95-910a-518eb226c896
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ondansetron hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA077851
- Marketing category
- ANDA
- Marketing start
- 2012-02-14
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record