Melphalan Hydrochloride
- Product NDC
- 70860-214
- 11-digit product format
- 708600214
- Labeler code
- 70860
- Product ID
- 70860-214_dd4de461-d51b-4f15-adac-568445d2b048
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- melphalan hydrochloride
- Dosage form
- KIT
- Route
- INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA209826
- Marketing category
- ANDA
- Marketing start
- 2019-07-30
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70860-214 | MELPHALAN HYDROCHLORIDE KIT [ATHENEX PHARMACEUTICAL DIVISION, LLC.] | 2 | Legacy NDC | 20240306_4ddcee81-7e3f-45c3-926e-8184e9679f86.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70860-214-61 | 70860021461 | 1 KIT in 1 CARTON (70860-214-61) * 10 mL in 1 VIAL, SINGLE-DOSE (70860-212-10) * 10 mL in 1 VIAL, SINGLE-USE (70860-213-10) | 1 kit | 2019-07-30 | 0000-00-00 | No | No | Current |