melphalan hydrochloride
- Product NDC
- 72611-779
- 11-digit product format
- 726110779
- Labeler code
- 72611
- Product ID
- 72611-779_2c93b457-205c-4e09-f8f3-a124f3a4c8d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- melphalan hydrochloride
- Dosage form
- KIT
- Labeler
- Almaject, Inc.
- Application
- ANDA204817
- Marketing category
- ANDA
- Marketing start
- 2019-05-18
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 72611-779 | MELPHALAN HYDROCHLORIDE KIT [ALMAJECT, INC.] | 5 | Legacy NDC | 20241122_a981ddb1-d05a-2cfe-10f5-1ce4dad8fe3c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72611-779-02 | 72611077902 | 1 KIT in 1 CARTON (72611-779-02) * 10 mL in 1 VIAL, SINGLE-DOSE (72611-772-01) * 10 mL in 1 VIAL, SINGLE-DOSE (72611-776-01) | 1 kit | 2020-11-01 | 0000-00-00 | No | No | Current |