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Approved Drug Products containing Denyl listed in the FDA Orange Book. Original Data : FDA Website

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02 1ACTAVIS MID ATLANTIC

03 1EPIC PHARMA LLC

04 1PAI HOLDINGS PHARM

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06 1RISING PHARMA

07 2VIATRIS

08 2VISTAPHARM

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PharmaCompass

01

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PHENYTOIN

Brand Name : PHENYTOIN

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 125MG/5ML

Approval Date : 2004-03-08

Application Number : 40521

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

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PHENYTOIN

Brand Name : PHENYTOIN

Dosage Form : TABLET, CHEWABLE;ORAL

Dosage Strength : 50MG

Approval Date : 2014-04-17

Application Number : 200565

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

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PHENYTOIN

Brand Name : PHENYTOIN

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 125MG/5ML

Approval Date : 1992-09-25

Application Number : 89892

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

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PHENYTOIN

Brand Name : PHENYTOIN

Dosage Form : TABLET, CHEWABLE;ORAL

Dosage Strength : 50MG

Approval Date : 2014-11-28

Application Number : 40884

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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05

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PHENYTOIN

Brand Name : PHENYTOIN

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 125MG/5ML

Approval Date : 2002-04-19

Application Number : 40420

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

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PHENYTOIN

Brand Name : DILANTIN

Dosage Form : TABLET, CHEWABLE;ORAL

Dosage Strength : 50MG

Approval Date : 1982-01-01

Application Number : 84427

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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07

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PHENYTOIN

Brand Name : DILANTIN-125

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 125MG/5ML

Approval Date : 1982-01-01

Application Number : 8762

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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08

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PHENYTOIN

Brand Name : DILANTIN-30

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 30MG/5ML

Approval Date : 1982-01-01

Application Number : 8762

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

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PHENYTOIN

Brand Name : PHENYTOIN

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 125MG/5ML

Approval Date : 2001-01-31

Application Number : 40342

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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PHENYTOIN

Brand Name : PHENYTOIN

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 125MG/5ML

Approval Date : 2005-08-18

Application Number : 40342

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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