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Dexrazoxane
Dexrazoxane - 55390-060-02 - (Dexrazoxane hydrochloride)
Drug Information of Dexrazoxane
| Product NDC: | 55390-060 |
| Proprietary Name: | Dexrazoxane |
| Non Proprietary Name: | Dexrazoxane hydrochloride |
| Active Ingredient(s): | & nbsp; Dexrazoxane hydrochloride |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dexrazoxane
| Product NDC: | 55390-060 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076068 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050331 |
Package Information of Dexrazoxane
| Package NDC: | 55390-060-02 |
| Package Description: | 1 KIT in 1 PACKAGE (55390-060-02) * 50 mL in 1 VIAL * 50 mL in 1 VIAL (55390-061-01) |
NDC Information of Dexrazoxane
| NDC Code | 55390-060-02 |
| Proprietary Name | Dexrazoxane |
| Package Description | 1 KIT in 1 PACKAGE (55390-060-02) * 50 mL in 1 VIAL * 50 mL in 1 VIAL (55390-061-01) |
| Product NDC | 55390-060 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dexrazoxane hydrochloride |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20050331 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
