Zinecard
- Product NDC
- 0013-8717
- 11-digit product format
- 000138717
- Labeler code
- 0013
- Product ID
- 0013-8717_c1ba93f1-2ec9-4787-b2ff-206499fee628
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dexrazoxane
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Pharmacia and Upjohn Company LLC
- Application
- NDA020212
- Marketing category
- NDA
- Marketing start
- 1995-05-26
- Marketing end
- 2021-04-30
- Substance
- DEXRAZOXANE HYDROCHLORIDE
- Active strength
- 250 mg/25mL
- Pharmacologic classes
- Cytoprotective Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0013-8717-62 | 00013871762 | 1 VIAL, SINGLE-DOSE in 1 CARTON (0013-8717-62) > 25 mL in 1 VIAL, SINGLE-DOSE | 1995-05-26 | 2021-04-30 | No | No | Current |