Phenytoin
NDC 51672-4069 · Sun Pharmaceutical Industries, Inc.
Generic namePhenytoin
Dosage formSUSPENSION
RouteORAL
Active ingredient(s)PHENYTOIN
Strength125 mg/5mL
Pharmacologic classAnti-epileptic Agent [EPC], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]
Marketing categoryANDA
Packages
51672-4069-2 — 1 BOTTLE in 1 CARTON (51672-4069-2) / 237 mL in 1 BOTTLE
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0071-0007 — Phenytoin, 0121-0892 — Phenytoin, 0615-8424 — Phenytoin, 0615-8623 — Phenytoin, 0904-7199 — Phenytoin, 17856-4070 — Phenytoin, 51672-4146 — Phenytoin, 58151-115 — Phenytoin, 59762-0531 — Phenytoin, 60687-156 — Phenytoin, 60687-275 — Phenytoin, 64980-573 — Phenytoin, 66993-372 — Phenytoin, 70518-0841 — Phenytoin