ONDANSETRON
- Product NDC
- 70518-2650
- 11-digit product format
- 705182650
- Labeler code
- 70518
- Product ID
- 70518-2650_dc787b11-439d-4f0e-e053-2995a90aadc0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ONDANSETRON
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203711
- Marketing category
- ANDA
- Marketing start
- 2020-03-25
- 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
- 2023-12-31
- 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 |
|---|
| 70518-2650-0 | 70518265000 | 25 VIAL, SINGLE-USE in 1 CARTON (70518-2650-0) > 2 mL in 1 VIAL, SINGLE-USE (70518-2650-1) | 2020-03-25 | 0000-00-00 | No | No | Current |