Docetaxel
- Product NDC
- 70700-174
- 11-digit product format
- 707000174
- Labeler code
- 70700
- Product ID
- 70700-174_5b73d1bb-972d-7aca-01d4-7564ef7d1849
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Docetaxel
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Xiromed LLC
- Application
- ANDA213510
- Marketing category
- ANDA
- Marketing start
- 2021-10-25
- Marketing end
- 0000-00-00
- Substance
- DOCETAXEL ANHYDROUS
- Active strength
- 10 mg/mL
- 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 |
|---|
| 70700-174-22 | 70700017422 | 1 VIAL, SINGLE-DOSE in 1 CARTON (70700-174-22) > 2 mL in 1 VIAL, SINGLE-DOSE | 2021-07-16 | 0000-00-00 | No | No | Current |