Paclitaxel
- Product NDC
- 69539-159
- 11-digit product format
- 695390159
- Labeler code
- 69539
- Product ID
- 69539-159_31f88042-2842-4bbb-9075-1fadffef637b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Paclitaxel
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- MSN LABORATORIES PRIVATE LIMITED
- Application
- ANDA213434
- Marketing category
- ANDA
- Marketing start
- 2020-08-26
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69539-159 | PACLITAXEL INJECTION, SOLUTION [MSN LABORATORIES PRIVATE LIMITED] | 3 | Legacy NDC | 20210728_2ca3c0d4-e629-4d89-a969-3515a62886c6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69539-159-01 | 69539015901 | 1 VIAL, MULTI-DOSE in 1 CARTON (69539-159-01) > 50 mL in 1 VIAL, MULTI-DOSE | 2020-08-26 | 0000-00-00 | No | No | Current |