NDC 51672-4111 – Phenytoin Sodium

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

Human Prescription Drug

Product NDC51672-4111

Product details

Brand name
Phenytoin Sodium
Generic name
Phenytoin Sodium
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA040684
Marketed since
September 5, 2006
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Phenytoin Sodium →

Package NDC codes (3)

Package NDCDescriptionSince
51672-4111-1100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51672-4111-1)Sep 5, 2006
51672-4111-31000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51672-4111-3)Sep 5, 2006
51672-4111-630 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51672-4111-6)Sep 5, 2006

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