Docetaxel anhydrous
- Product NDC
- 71288-143
- 11-digit product format
- 712880143
- Labeler code
- 71288
- Product ID
- 71288-143_bde535be-817f-4e14-e053-2a95a90a7b4f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Docetaxel anhydrous
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Meitheal Pharmaceuticals Inc
- Application
- ANDA209634
- Marketing category
- ANDA
- Marketing start
- 2018-08-24
- Marketing end
- 0000-00-00
- Substance
- DOCETAXEL ANHYDROUS
- Active strength
- 20 mg/2mL
- Pharmacologic classes
- Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 71288-143-02 | 71288014302 | 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-143-02) > 2 mL in 1 VIAL, SINGLE-DOSE | 2018-08-24 | 0000-00-00 | No | No | Current |