Paclitaxel
- Product NDC
- 67457-471
- 11-digit product format
- 674570471
- Labeler code
- 67457
- Product ID
- 67457-471_3346469b-10d5-42ef-ac5a-aeb1c720548a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Paclitaxel
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA091540
- Marketing category
- ANDA
- Marketing start
- 2014-08-07
- Marketing end
- 2021-02-28
- Substance
- PACLITAXEL
- Active strength
- 30 mg/5mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67457-471-52 | 67457047152 | 1 VIAL in 1 CARTON (67457-471-52) > 5 mL in 1 VIAL | 1 vial | 2014-08-07 | 2021-02-28 | No | No | Current |