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fosphenytoin sodium
fosphenytoin sodium - 0517-6902-10 - (fosphenytoin sodium)
Drug Information of fosphenytoin sodium
| Product NDC: | 0517-6902 |
| Proprietary Name: | fosphenytoin sodium |
| Non Proprietary Name: | fosphenytoin sodium |
| Active Ingredient(s): | 50 mg/mL & nbsp; fosphenytoin sodium |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of fosphenytoin sodium
| Product NDC: | 0517-6902 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090099 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100730 |
Package Information of fosphenytoin sodium
| Package NDC: | 0517-6902-10 |
| Package Description: | 10 VIAL in 1 BOX (0517-6902-10) > 2 mL in 1 VIAL |
NDC Information of fosphenytoin sodium
| NDC Code | 0517-6902-10 |
| Proprietary Name | fosphenytoin sodium |
| Package Description | 10 VIAL in 1 BOX (0517-6902-10) > 2 mL in 1 VIAL |
| Product NDC | 0517-6902 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fosphenytoin sodium |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20100730 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | FOSPHENYTOIN SODIUM |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
