MELPHALAN HYDROCHLORIDE
- Product NDC
- 50742-477
- 11-digit product format
- 507420477
- Labeler code
- 50742
- Product ID
- 50742-477_3b2a817f-1584-4a77-8c2c-a89373542731
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MELPHALAN HYDROCHLORIDE
- Dosage form
- KIT
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA210947
- Marketing category
- ANDA
- Marketing start
- 2020-02-18
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50742-477-01 | 50742047701 | 1 KIT in 1 CARTON (50742-477-01) * 10 mL in 1 VIAL, SINGLE-DOSE (50742-475-10) * 10 mL in 1 VIAL, SINGLE-DOSE (50742-476-10) | 1 kit | 2020-02-18 | 0000-00-00 | No | No | Current |