Palonosetron Hydrochloride
- Product NDC
- 50742-485
- 11-digit product format
- 507420485
- Labeler code
- 50742
- Product ID
- 50742-485_1a1adc8f-0e7c-4e64-b9f4-7b625686c142
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Palonosetron Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA208789
- Marketing category
- ANDA
- Marketing start
- 2020-05-29
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- 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 |
|---|
| 50742-485-05 | 50742048505 | 1 VIAL in 1 CARTON (50742-485-05) > 5 mL in 1 VIAL | 1 vial | 2020-05-29 | 0000-00-00 | No | No | Current |