Phenytoin 51672-4146
Product NDC
51672-4146- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 17, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA200565
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Phenytoin | 50 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Anti-epileptic Agent [EPC]Cytochrome P450 1A2 Inducers [MoA]
Packaging Options(3)
100 TABLET, CHEWABLE in 1 BOTTLE (51672-4146-1)
1000 TABLET, CHEWABLE in 1 BOTTLE (51672-4146-3)
30 TABLET, CHEWABLE in 1 BOTTLE (51672-4146-6)