NDC 58151-110 – Dilantin

Phenytoin Sodium 100 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC58151-110

Product details

Brand name
Dilantin
Generic name
Extended Phenytoin Sodium
Labeler
Viatris Specialty LLC
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA084349
Marketed since
December 6, 2024
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Dilantin →

Package NDC codes (3)

Package NDCDescriptionSince
58151-110-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (58151-110-01)Dec 6, 2024
58151-110-101000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (58151-110-10)Apr 9, 2025
58151-110-88100 BLISTER PACK in 1 CARTON (58151-110-88) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (58151-110-32)Dec 6, 2024

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