Paclitaxel
- Product NDC
- 68001-705
- 11-digit product format
- 680010705
- Labeler code
- 68001
- Product ID
- 68001-705_523b8199-fcb1-57d3-e063-6294a90aabca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Paclitaxel
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- BluePoint Laboratories
- Application
- ANDA216874
- Marketing category
- ANDA
- Marketing start
- 2026-04-01
- Substance
- PACLITAXEL
- Active strength
- 6 mg/mL
- Pharmacologic classes
- Microtubule Inhibition [PE], Microtubule Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Paclitaxel
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PACLITAXEL | 6 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | P88XT4IS4D |
| Rxcui | 312199 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68001-705-27 | Paclitaxel | 50 mL in 1 VIAL, MULTI-DOSE | INJECTION | 50 | | 2 |
| 68001-705-27 | Paclitaxel | 1 in 1 CARTON | INJECTION | 1 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68001-705-27 | 68001070527 | 1 VIAL, MULTI-DOSE in 1 CARTON (68001-705-27) / 50 mL in 1 VIAL, MULTI-DOSE | 2026-04-09 | No | No | Historical |