Docetaxel
- Product NDC
- 66758-950
- 11-digit product format
- 667580950
- Labeler code
- 66758
- Product ID
- 66758-950_f161a570-3193-49b4-b2e9-fee4d17404f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- docetaxel
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sandoz Inc.
- Application
- NDA201525
- Marketing category
- NDA
- Marketing start
- 2015-07-22
- Marketing end
- 0000-00-00
- Substance
- DOCETAXEL
- Active strength
- 10 mg/mL
- 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 |
|---|
| 66758-950-02 | 66758095002 | 1 VIAL, MULTI-DOSE in 1 CARTON (66758-950-02) > 2 mL in 1 VIAL, MULTI-DOSE | 2015-07-22 | 0000-00-00 | No | No | Current |
| 66758-950-03 | 66758095003 | 1 VIAL, MULTI-DOSE in 1 CARTON (66758-950-03) > 8 mL in 1 VIAL, MULTI-DOSE | 2015-07-22 | 0000-00-00 | No | No | Current |
| 66758-950-04 | 66758095004 | 1 VIAL, MULTI-DOSE in 1 CARTON (66758-950-04) > 16 mL in 1 VIAL, MULTI-DOSE | 2015-07-22 | 0000-00-00 | No | No | Current |