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01 1AM REGENT

02 1AMNEAL

03 6ANI PHARMS

04 2BIONPHARMA

05 1CHENGDU SHUODE

06 10CHIESI

07 2CIPLA

08 2EPIC PHARMA LLC

09 1EUGIA PHARMA

10 2GLENMARK PHARMS LTD

11 3HIKMA INTL PHARMS

12 2INFORLIFE

13 1MICRO LABS

14 1NAVINTA LLC

15 2NORVIUM BIOSCIENCE

16 1RK PHARMA

17 2SENORES PHARMS

18 2SKG PHARMA

19 1SUN PHARM

20 1WEST-WARD PHARMS INT

21 1WOCKHARDT

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PharmaCompass

01

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1988-12-21

Application Number : 19488

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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02

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1988-12-21

Application Number : 19488

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 25MG/10ML (2.5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-01-30

Application Number : 19734

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE IN 4.8% DEXTROSE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : 20MG/200ML (0.1MG/ML)

Approval Date : 2008-07-31

Application Number : 19734

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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05

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE IN 0.86% SODIUM CHLORIDE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : 20MG/200ML (0.1MG/ML)

Approval Date : 2008-07-31

Application Number : 19734

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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06

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE IN 0.83% SODIUM CHLORIDE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : 40MG/200ML (0.2MG/ML)

Approval Date : 2008-11-07

Application Number : 19734

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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07

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE IN 5.0% DEXTROSE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : 40MG/200ML (0.2MG/ML)

Approval Date : 2008-11-07

Application Number : 19734

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE SR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-02-21

Application Number : 20005

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

Antibody Engineering
Not Confirmed
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Antibody Engineering
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE SR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 45MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-02-21

Application Number : 20005

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

Antibody Engineering
Not Confirmed
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arrow
Antibody Engineering
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE SR

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-02-21

Application Number : 20005

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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