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Zinecard
Zinecard - 0013-8727-89 - (dexrazoxane)
Drug Information of Zinecard
| Product NDC: | 0013-8727 |
| Proprietary Name: | Zinecard |
| Non Proprietary Name: | dexrazoxane |
| Active Ingredient(s): | & nbsp; dexrazoxane |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zinecard
| Product NDC: | 0013-8727 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020212 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19950526 |
Package Information of Zinecard
| Package NDC: | 0013-8727-89 |
| Package Description: | 1 KIT in 1 PACKAGE (0013-8727-89) * 50 mL in 1 VIAL * 50 mL in 1 VIAL |
NDC Information of Zinecard
| NDC Code | 0013-8727-89 |
| Proprietary Name | Zinecard |
| Package Description | 1 KIT in 1 PACKAGE (0013-8727-89) * 50 mL in 1 VIAL * 50 mL in 1 VIAL |
| Product NDC | 0013-8727 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dexrazoxane |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19950526 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
