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Dexrazoxane Hydrochloride
Dexrazoxane Hydrochloride - 67457-208-50 - (dexrazoxane)
Drug Information of Dexrazoxane Hydrochloride
| Product NDC: | 67457-208 |
| Proprietary Name: | Dexrazoxane Hydrochloride |
| 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 Dexrazoxane Hydrochloride
| Product NDC: | 67457-208 |
| Labeler Name: | Mylan Institutional LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200752 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121114 |
Package Information of Dexrazoxane Hydrochloride
| Package NDC: | 67457-208-50 |
| Package Description: | 1 KIT in 1 PACKAGE (67457-208-50) * 50 mL in 1 VIAL, SINGLE-DOSE (67457-209-50) * 50 mL in 1 VIAL (67457-205-50) |
NDC Information of Dexrazoxane Hydrochloride
| NDC Code | 67457-208-50 |
| Proprietary Name | Dexrazoxane Hydrochloride |
| Package Description | 1 KIT in 1 PACKAGE (67457-208-50) * 50 mL in 1 VIAL, SINGLE-DOSE (67457-209-50) * 50 mL in 1 VIAL (67457-205-50) |
| Product NDC | 67457-208 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dexrazoxane |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20121114 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
