Product NDC: | 0641-2555 |
Proprietary Name: | Phenytoin Sodium |
Non Proprietary Name: | Phenytoin Sodium |
Active Ingredient(s): | 50 mg/mL & nbsp; Phenytoin Sodium |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0641-2555 |
Labeler Name: | West-Ward Pharmaceutical Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA084307 |
Marketing Category: | ANDA |
Start Marketing Date: | 19750716 |
Package NDC: | 0641-2555-45 |
Package Description: | 25 VIAL in 1 CARTON (0641-2555-45) > 5 mL in 1 VIAL (0641-2555-41) |
NDC Code | 0641-2555-45 |
Proprietary Name | Phenytoin Sodium |
Package Description | 25 VIAL in 1 CARTON (0641-2555-45) > 5 mL in 1 VIAL (0641-2555-41) |
Product NDC | 0641-2555 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Phenytoin Sodium |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 19750716 |
Marketing Category Name | ANDA |
Labeler Name | West-Ward Pharmaceutical Corp. |
Substance Name | PHENYTOIN SODIUM |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |