Palonosetron
- Product NDC
- 68001-482
- 11-digit product format
- 680010482
- Labeler code
- 68001
- Product ID
- 68001-482_ecf9957d-55d8-6f94-e053-2995a90a6cba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Palonosetron Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- BluePoint Laboratories
- Application
- ANDA205648
- Marketing category
- ANDA
- Marketing start
- 2021-01-25
- Marketing end
- 2023-07-31
- Substance
- PALONOSETRON HYDROCHLORIDE
- Active strength
- 0 mg/5mL
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-482-25 | 68001048225 | 1 VIAL in 1 CARTON (68001-482-25) > 5 mL in 1 VIAL | 1 vial | 2021-01-25 | 0000-00-00 | No | No | Current |