ONDANSETRON
- Product NDC
- 68071-4191
- 11-digit product format
- 680714191
- Labeler code
- 68071
- Product ID
- 68071-4191_60683674-eae5-2745-e053-2991aa0a81e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ONDANSETRON
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA079224
- Marketing category
- ANDA
- Marketing start
- 2012-06-15
- 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