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NDC 17856-4070-01 Phenytoin 125 mg/5mL Details

Phenytoin 125 mg/5mL

Phenytoin is a ORAL SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ATLANTIC BIOLOGICALS CORP.. The primary component is PHENYTOIN.

MedlinePlus Drug Summary

Phenytoin is used to control certain type of seizures, and to treat and prevent seizures that may begin during or after surgery to the brain or nervous system. Phenytoin is in a class of medications called anticonvulsants. It works by decreasing abnormal electrical activity in the brain.

Related Packages: 17856-4070-01
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Phenytoin

Product Information

NDC	17856-4070
Product ID	17856-4070_c459d001-5e1e-4122-a016-18ed7de1abef
Associated GPIs
GCN Sequence Number	063845
GCN Sequence Number Description	phenytoin ORAL SUSP 100 MG/4ML ORAL
HIC3	H4B
HIC3 Description	ANTICONVULSANTS
GCN	99557
HICL Sequence Number	001879
HICL Sequence Number Description	PHENYTOIN
Brand/Generic	Generic
Proprietary Name	Phenytoin
Proprietary Name Suffix	n/a
Non-Proprietary Name	Phenytoin
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	SUSPENSION
Route	ORAL
Active Ingredient Strength	125
Active Ingredient Units	mg/5mL
Substance Name	PHENYTOIN
Labeler Name	ATLANTIC BIOLOGICALS CORP.
Pharmaceutical Class	Anti-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
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA040521
Listing Certified Through	2022-12-31

Package

NDC 17856-4070-01 (17856407001)

Pricing Information	N/A
NDC Package Code	17856-4070-1
Billing NDC	17856407001
Package	72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-4070-1) / 4 mL in 1 CUP, UNIT-DOSE (17856-4070-2)
Marketing Start Date	2022-11-30
NDC Exclude Flag	N