Phenytoin - PHENYTOIN
Navigation: NDC > Supplier starting with: G > GREENSTONE LLC| Field | Value |
|---|---|
| NDC Code: | 59762-0531 |
| Proprietary Name: | Phenytoin |
| Suffix: | |
| Non-Proprietary Name: | PHENYTOIN |
| Dosage Form: | SUSPENSION |
| Method: | ORAL |
| Original Marketing Date: | 01-10-2012 |
| Category Name: | NDA AUTHORIZED GENERIC |
| Application Number: | NDA008762 |
| Labeler: | GREENSTONE LLC |
| Substance Name: | PHENYTOIN |
| Active Numerator Strength: | 125 |
| Active Ingredient Unit: | mg/5mL |
| Pharm Classes: | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
| DEA Schedule: |