Paclitaxel
- Product NDC
- 47781-595
- 11-digit product format
- 477810595
- Labeler code
- 47781
- Product ID
- 47781-595_a0a20ab5-3187-2675-9eff-f4fac3dc89bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- paclitaxel
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Alvogen Inc.
- Application
- ANDA207326
- Marketing category
- ANDA
- Marketing start
- 2017-12-27
- Marketing end
- 0000-00-00
- Substance
- PACLITAXEL
- Active strength
- 300 mg/50mL
- Pharmacologic classes
- Microtubule Inhibition [PE], Microtubule Inhibitor [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 |
|---|
| 47781-595-07 | 47781059507 | 1 VIAL, MULTI-DOSE in 1 CARTON (47781-595-07) > 50 mL in 1 VIAL, MULTI-DOSE | 2017-12-27 | 0000-00-00 | No | No | Current |