Paclitaxel
- Product NDC
- 47781-594
- 11-digit product format
- 477810594
- Labeler code
- 47781
- Product ID
- 47781-594_1979e29d-1ab0-ddd7-b39f-6fdc86a8d0b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- paclitaxel
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Alvogen Inc.
- Application
- ANDA207326
- Marketing category
- ANDA
- Marketing start
- 2017-12-27
- Marketing end
- 2020-01-01
- Substance
- PACLITAXEL
- Active strength
- 100 mg/16.7mL
- 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