Paclitaxel
- Product NDC
- 44567-505
- 11-digit product format
- 445670505
- Labeler code
- 44567
- Product ID
- 44567-505_e4365bc6-3216-420b-aef2-12439a8033ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Paclitaxel
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- WG Critical Care, LLC
- Application
- NDA020262
- Marketing category
- NDA
- Marketing start
- 2013-07-11
- Marketing end
- 2022-04-30
- Substance
- PACLITAXEL
- Active strength
- 6 mg/mL
- Pharmacologic classes
- Microtubule Inhibition [PE],Microtubule Inhibitor [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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44567-505-01 | 44567050501 | 1 VIAL, MULTI-DOSE in 1 CARTON (44567-505-01) > 16.7 mL in 1 VIAL, MULTI-DOSE | 2013-07-11 | 0000-00-00 | No | No | Current |