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01 1MANKIND PHARMA

02 1CHENGDU SHUODE

03 1AM REGENT

04 3AMNEAL

05 6ANI PHARMS

06 2BIONPHARMA

07 2CAPLIN

08 10CHIESI

09 2CIPLA

10 2EPIC PHARMA LLC

11 1EUGIA PHARMA

12 2GLENMARK PHARMS LTD

13 1HIKMA

14 3HIKMA INTL PHARMS

15 2INFORLIFE

16 1MICRO LABS

17 1NANJING KING FRIEND

18 3NAVINTA LLC

19 2PHARMOBEDIENT

20 1QILU PHARM HAINAN

21 2SENORES PHARMS

22 1SOMERSET THERAPS LLC

23 1SUN PHARM

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AP

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 25MG/10ML (2.5MG/ML)

Approval Date : 2009-11-17

Application Number : 90671

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothQingmu Pharma: Patients first, FDA/CEP/US-DMF/US-VMF/ASMF APIs for Humans & Vets in 100+ countries.

RLD : No

TE Code : AP

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 25MG/10ML (2.5MG/ML)

Approval Date : 2024-09-06

Application Number : 217548

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

Company Banner

03

ASCO GU
Not Confirmed
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ASCO GU
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Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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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04

ASCO GU
Not Confirmed
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ASCO GU
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Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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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05

ASCO GU
Not Confirmed
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ASCO GU
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 25MG/10ML (2.5MG/ML)

Approval Date : 1992-01-30

Application Number : 19734

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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06

ASCO GU
Not Confirmed
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ASCO GU
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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07

ASCO GU
Not Confirmed
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ASCO GU
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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08

ASCO GU
Not Confirmed
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ASCO GU
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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09

ASCO GU
Not Confirmed
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ASCO GU
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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10

ASCO GU
Not Confirmed
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ASCO GU
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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