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phenytoin sodium

NDC 62756-432 · Sun Pharmaceutical Industries, Inc.

Generic namephenytoin sodium
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Active ingredient(s)PHENYTOIN SODIUM
Strength300 mg/1
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

62756-432-08 — 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-432-08)

62756-432-13 — 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-432-13)

62756-432-83 — 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-432-83)

62756-432-88 — 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-432-88)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50268-719 — Phenytoin Sodium, 51407-982 — Phenytoin Sodium, 51662-1250 — PHENYTOIN SODIUM, 51662-1251 — PHENYTOIN SODIUM, 51672-4111 — Phenytoin Sodium, 58151-110 — Extended Phenytoin Sodium, 58151-118 — Extended Phenytoin Sodium, 60687-841 — Phenytoin Sodium, 61919-815 — PHENYTOIN SODIUM, 62756-299 — phenytoin sodium, 65162-212 — Phenytoin Sodium, 65862-692 — Phenytoin Sodium, 67046-0585 — Phenytoin Sodium, 67046-1486 — extended phenytoin sodium, 70518-0107 — Phenytoin Sodium, 70518-2227 — Phenytoin Sodium, 70518-2293 — Phenytoin Sodium, 70518-4325 — Extended Phenytoin Sodium, 71610-869 — Phenytoin Sodium, 71610-934 — Phenytoin Sodium, +19 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.