Palonosetron Hydrochloride
- Product NDC
- 70860-785
- 11-digit product format
- 708600785
- Labeler code
- 70860
- Product ID
- 70860-785_b28082d9-2928-45b9-826a-19c4dec8fc79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- palonosetron hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA202951
- Marketing category
- ANDA
- Marketing start
- 2022-10-01
- Marketing end
- 0000-00-00
- Substance
- PALONOSETRON HYDROCHLORIDE
- Active strength
- 0 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 |
|---|
| 70860-785-05 | 70860078505 | 1 VIAL, SINGLE-DOSE in 1 CARTON (70860-785-05) > 5 mL in 1 VIAL, SINGLE-DOSE | 2022-10-01 | 0000-00-00 | No | No | Current |