| NDC Code: |
47335-833 |
| Proprietary Name: |
Fosphenytoin Sodium |
| Suffix: |
|
| Non-Proprietary Name: |
Fosphenytoin Sodium |
| Dosage Form: |
INJECTION, SOLUTION |
| Method: |
INTRAMUSCULAR; INTRAVENOUS |
| Original Marketing Date: |
14-08-2009 |
| Category Name: |
ANDA |
| Application Number: |
ANDA078417 |
| Labeler: |
SUN PHARMA GLOBAL FZE |
| Substance Name: |
FOSPHENYTOIN SODIUM |
| Active Numerator Strength: |
50 |
| Active Ingredient Unit: |
mg/mL |
| Pharm Classes: |
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
| DEA Schedule: |
|
