Paclitaxel
- Product NDC
- 0703-4768
- 11-digit product format
- 007034768
- Labeler code
- 0703
- Product ID
- 0703-4768_0b02547e-0b69-4044-9495-f5b7f287e2c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Paclitaxel
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Teva Parenteral Medicines, Inc.
- Application
- ANDA075184
- Marketing category
- ANDA
- Marketing start
- 2016-03-03
- Marketing end
- 0000-00-00
- Substance
- PACLITAXEL
- Active strength
- 6 mg/mL
- Pharmacologic classes
- Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 0703-4768-81 | 00703476881 | 1 VIAL, MULTI-DOSE in 1 CARTON (0703-4768-81) > 50 mL in 1 VIAL, MULTI-DOSE | 2016-03-03 | 0000-00-00 | No | No | Current |