Docetaxel
- Product NDC
- 45963-790
- 11-digit product format
- 459630790
- Labeler code
- 45963
- Product ID
- 45963-790_5a6c204e-5b3b-40fc-b007-a4d21ae6c406
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Docetaxel
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Actavis Pharma, Inc.
- Application
- NDA203551
- Marketing category
- NDA
- Marketing start
- 2015-10-13
- Marketing end
- 2021-02-28
- Substance
- DOCETAXEL
- Active strength
- 20 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 |
|---|
| 45963-790-56 | 45963079056 | 1 VIAL, GLASS in 1 CARTON (45963-790-56) > 8 mL in 1 VIAL, GLASS | 2015-10-13 | 2021-02-28 | No | No | Current |