NDCFind

Phenytoin 51672-4069-02

Package NDC

51672-4069-02

Product NDC: 51672-4069

Manufacturer
Sun Pharmaceutical Industries, Inc.
Dosage Form
Suspension
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
April 8, 2004
Listing Expires
December 31, 2026
Application
ANDA040521
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Active Ingredients

IngredientStrength
Phenytoin125 mg/5mL

Drug Class

Anti-epileptic Agent [EPC]Anti-epileptic Agent [EPC]Cytochrome P450 1A2 Inducers [MoA]

Selected Package

51672-4069-02Selected

1 BOTTLE in 1 CARTON (51672-4069-2) / 237 mL in 1 BOTTLE

Other packages for this product(1)

237 mL in 1 BOTTLE (51672-4069-1)