NDC 17856-4070 – Phenytoin

Phenytoin 125 mg/5mL · Suspension · Oral

Human Prescription Drug

Product NDC17856-4070

Product details

Brand name
Phenytoin
Generic name
Phenytoin
Labeler
ATLANTIC BIOLOGICALS CORP.
Dosage form
Suspension
Route
Oral
Marketing category
ANDA · ANDA040521
Marketed since
April 8, 2004
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Phenytoin →

Package NDC codes (1)

Package NDCDescriptionSince
17856-4070-172 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-4070-1) / 4 mL in 1 CUP, UNIT-DOSE (17856-4070-2)May 9, 2024

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