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Approved Drug Products containing DSSTox_CID_3551 listed in the FDA Orange Book. Original Data : FDA Website

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01 4ACCORD HLTHCARE

02 4ACTAVIS ELIZABETH

03 4APOTEX

04 4AUROBINDO PHARMA LTD

05 4CHARTWELL MOLECULAR

06 4CHARTWELL RX

07 4CIPLA

08 4COREPHARMA

09 4DR REDDYS LABS LTD

10 4HIKMA

11 4KING PFIZER

12 4KING PHARMS LLC

13 4LUPIN

14 4NATCO PHARMA

15 2RANBAXY LABS LTD

16 4TEVA PHARMS

17 4WATSON LABS

18 4ZYDUS PHARMS USA

19 4ZYDUS PHARMS USA INC

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PharmaCompass

01

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RAMIPRIL

Brand Name : RAMIPRIL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 1.25MG

Approval Date : 2005-10-24

Application Number : 76549

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

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RAMIPRIL

Brand Name : RAMIPRIL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 2.5MG

Approval Date : 2005-10-24

Application Number : 76549

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

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RAMIPRIL

Brand Name : ALTACE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 1.25MG

Approval Date : 1991-01-28

Application Number : 19901

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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04

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RAMIPRIL

Brand Name : ALTACE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 2.5MG

Approval Date : 1991-01-28

Application Number : 19901

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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05

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RAMIPRIL

Brand Name : ALTACE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 5MG

Approval Date : 1991-01-28

Application Number : 19901

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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06

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RAMIPRIL

Brand Name : ALTACE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 10MG

Approval Date : 1991-01-28

Application Number : 19901

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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07

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RAMIPRIL

Brand Name : ALTACE

Dosage Form : TABLET;ORAL

Dosage Strength : 1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2007-02-27

Application Number : 22021

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

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RAMIPRIL

Brand Name : ALTACE

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2007-02-27

Application Number : 22021

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

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RAMIPRIL

Brand Name : ALTACE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2007-02-27

Application Number : 22021

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

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RAMIPRIL

Brand Name : ALTACE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2007-02-27

Application Number : 22021

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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