VINORELBINE
- Product NDC
- 61703-341
- 11-digit product format
- 617030341
- Labeler code
- 61703
- Product ID
- 61703-341_7133a031-8cfa-4c67-8c09-12711a45184a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vinorelbine
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- ANDA076827
- Marketing category
- ANDA
- Marketing start
- 2007-04-02
- Marketing end
- 2019-05-31
- Substance
- VINORELBINE TARTRATE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Vinca Alkaloid [EPC],Vinca Alkaloids [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record