Dexrazoxane Hydrochloride
- Product NDC
- 67457-207
- 11-digit product format
- 674570207
- Labeler code
- 67457
- Product ID
- 67457-207_d0adbbbb-703c-47d2-85d3-e2f8949b81fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dexrazoxane
- Dosage form
- KIT
- Labeler
- Mylan Institutional LLC
- Application
- ANDA200752
- Marketing category
- ANDA
- Marketing start
- 2011-11-18
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67457-207-25 | 67457020725 | 1 KIT in 1 PACKAGE (67457-207-25) * 25 mL in 1 VIAL (67457-205-25) * 25 mL in 1 VIAL, SINGLE-DOSE (67457-204-25) | 1 kit | 2011-11-18 | 0000-00-00 | No | No | Current |