MELPHALAN HYDROCHLORIDE
- Product NDC
- 70700-278
- 11-digit product format
- 707000278
- Labeler code
- 70700
- Product ID
- 70700-278_bd5d2c52-f90f-7776-177d-4bc15dfba8e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MELPHALAN HYDROCHLORIDE
- Dosage form
- KIT
- Labeler
- Xiromed, LLC
- Application
- ANDA210947
- Marketing category
- ANDA
- Marketing start
- 2021-01-06
- 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 |
|---|
| 70700-278-97 | 70700027897 | 1 KIT in 1 CARTON (70700-278-97) * 10 mL in 1 VIAL, SINGLE-DOSE (70700-277-22) * 10 mL in 1 VIAL, SINGLE-DOSE (70700-276-96) | 1 kit | 2021-01-06 | 0000-00-00 | No | No | Current |