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01 1Octavius Pharma Pvt. Ltd

02 1Mankind Pharma

03 1Lee Pharma

04 1Sichuan Qingmu Pharmaceutical

05 2ACS DOBFAR SPA

06 6ANI Pharmaceuticals Inc

07 1American Regent

08 1Amneal Pharmaceuticals

09 1Amospharm

10 2Anwita Drugs

11 1Aurobindo Pharma Limited

12 2Bionpharma

13 10CHIESI USA INC

14 2Cipla

15 1Clinigen Group

16 1Cooper Pharma Limited

17 1Deva Holding AS

18 2Epic Pharma. LLC.

19 4Farbe Firma

20 2Glenmark Pharmaceuticals

21 1Ha Noi CPC1 Pharmaceutical JSC

22 4Hikma Pharmaceuticals

23 1Loxim Industries

24 1Micro Labs Limited

25 1Montage Laboratories

26 1Murli Krishna Pharma

27 3Navinta

28 2Norvium

29 1RK Pharma

30 2ROTTAPHARM SpA

31 1Ravoos Laboratories

32 2SKG-Pharma

33 2Senores Pharmaceuticals

34 1Sun Pharmaceutical Industries Limited

35 1Viatris

36 1Zhejiang Xianju Pharmaceutical Co. Ltd

37 2Blank

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothOctavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.

Regulatory Info :

Registration Country : India

Nicardipine Hydrochloride

Brand Name : Nicardipine

Dosage Form : Pellets for Capsules

Dosage Strength : 22%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

02

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : RX

Registration Country : USA

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

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

Packaging :

Approval Date : 2009-11-17

Application Number : 90671

Regulatory Info : RX

Registration Country : USA

Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothLee Pharma Ltd: Global supplier of certified APIs and formulations, driven by innovation and regulatory excellence.

Regulatory Info :

Registration Country : India

Nicardipine Hydrochloride

Brand Name : Nicardipine Hydrochloride

Dosage Form : Pellets

Dosage Strength :

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSichuan Qingmu Pharmaceutical offers reliable CDMO support and high-quality APIs for regulated markets.

Regulatory Info : RX

Registration Country : USA

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

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

Packaging :

Approval Date : 2024-09-06

Application Number : 217548

Regulatory Info : RX

Registration Country : USA

Company Banner

05

AGGSpend
Not Confirmed
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AGGSpend
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 1996-12-10

Application Number : 74439

Regulatory Info : DISCN

Registration Country : USA

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06

AGGSpend
Not Confirmed
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AGGSpend
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1996-12-10

Application Number : 74439

Regulatory Info : DISCN

Registration Country : USA

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07

AGGSpend
Not Confirmed
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AGGSpend
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 1996-10-28

Application Number : 74540

Regulatory Info : DISCN

Registration Country : USA

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08

AGGSpend
Not Confirmed
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AGGSpend
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**

Packaging :

Approval Date : 1988-12-21

Application Number : 19488

Regulatory Info : DISCN

Registration Country : USA

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09

AGGSpend
Not Confirmed
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AGGSpend
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**

Packaging :

Approval Date : 1988-12-21

Application Number : 19488

Regulatory Info : DISCN

Registration Country : USA

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10

AGGSpend
Not Confirmed
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AGGSpend
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**

Packaging :

Approval Date : 1992-01-30

Application Number : 19734

Regulatory Info : DISCN

Registration Country : USA

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11

AGGSpend
Not Confirmed
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AGGSpend
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)

Packaging :

Approval Date : 2008-07-31

Application Number : 19734

Regulatory Info : RX

Registration Country : USA

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12

AGGSpend
Not Confirmed
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AGGSpend
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)

Packaging :

Approval Date : 2008-07-31

Application Number : 19734

Regulatory Info : RX

Registration Country : USA

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13

AGGSpend
Not Confirmed
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AGGSpend
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)

Packaging :

Approval Date : 2008-11-07

Application Number : 19734

Regulatory Info : RX

Registration Country : USA

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14

AGGSpend
Not Confirmed
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AGGSpend
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)

Packaging :

Approval Date : 2008-11-07

Application Number : 19734

Regulatory Info : DISCN

Registration Country : USA

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15

AGGSpend
Not Confirmed
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AGGSpend
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**

Packaging :

Approval Date : 1992-02-21

Application Number : 20005

Regulatory Info : DISCN

Registration Country : USA

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16

AGGSpend
Not Confirmed
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AGGSpend
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**

Packaging :

Approval Date : 1992-02-21

Application Number : 20005

Regulatory Info : DISCN

Registration Country : USA

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17

AGGSpend
Not Confirmed
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AGGSpend
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**

Packaging :

Approval Date : 1992-02-21

Application Number : 20005

Regulatory Info : DISCN

Registration Country : USA

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18

AGGSpend
Not Confirmed
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AGGSpend
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

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

Packaging :

Approval Date : 2008-07-24

Application Number : 22276

Regulatory Info : RX

Registration Country : USA

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19

AGGSpend
Not Confirmed
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AGGSpend
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE

Dosage Form : INJECTABLE;INTRAVENOUS

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

Packaging :

Approval Date : 2016-04-07

Application Number : 22276

Regulatory Info : RX

Registration Country : USA

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20

AGGSpend
Not Confirmed
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AGGSpend
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE

Dosage Form : INJECTABLE;INTRAVENOUS

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

Packaging :

Approval Date : 2016-04-07

Application Number : 22276

Regulatory Info : RX

Registration Country : USA

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