Vinorelbine
- Product NDC
- 50742-420
- 11-digit product format
- 507420420
- Labeler code
- 50742
- Product ID
- 50742-420_b448ff8a-6196-49e3-bf8b-9615e87c837b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vinorelbine
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA208997
- Marketing category
- ANDA
- Marketing start
- 2019-08-08
- Marketing end
- 0000-00-00
- Substance
- VINORELBINE TARTRATE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Vinca Alkaloid [EPC],Vinca Alkaloids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 50742-420-01 | 50742042001 | 1 VIAL, SINGLE-USE in 1 CARTON (50742-420-01) > 1 mL in 1 VIAL, SINGLE-USE | 2019-08-08 | 0000-00-00 | No | No | Current |