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AMIFOSTINE
AMIFOSTINE - 47335-581-42 - (AMIFOSTINE)
Drug Information of AMIFOSTINE
| Product NDC: | 47335-581 |
| Proprietary Name: | AMIFOSTINE |
| Non Proprietary Name: | AMIFOSTINE |
| Active Ingredient(s): | 50 mg/mL & nbsp; AMIFOSTINE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AMIFOSTINE
| Product NDC: | 47335-581 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077126 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080314 |
Package Information of AMIFOSTINE
| Package NDC: | 47335-581-42 |
| Package Description: | 3 VIAL, SINGLE-USE in 1 CARTON (47335-581-42) > 10 mL in 1 VIAL, SINGLE-USE |
NDC Information of AMIFOSTINE
| NDC Code | 47335-581-42 |
| Proprietary Name | AMIFOSTINE |
| Package Description | 3 VIAL, SINGLE-USE in 1 CARTON (47335-581-42) > 10 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 47335-581 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AMIFOSTINE |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080314 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | AMIFOSTINE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
