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01 1Octavius Pharma Pvt. Ltd

02 1Mankind Pharma

03 1Sichuan Qingmu Pharmaceutical

04 2ACS DOBFAR SPA

05 6ANI Pharmaceuticals Inc

06 1Aguettant

07 1American Regent

08 3Amneal Pharmaceuticals

09 1Amospharm

10 2Anwita Drugs

11 1Aurobindo Pharma Limited

12 2Bionpharma

13 10CHIESI USA INC

14 2Caplin Point Laboratories Limited

15 2Cipla

16 1Clinigen Group

17 1Cooper Pharma Limited

18 1Deva Holding AS

19 2Epic Pharma. LLC.

20 4Farbe Firma

21 2Ferrer Internacional

22 2Glenmark Pharmaceuticals

23 1Ha Noi CPC1 Pharmaceutical JSC

24 4Hikma Pharmaceuticals

25 2Kern Pharma S.L.

26 1Micro Labs Limited

27 1Montage Laboratories

28 1Murli Krishna Pharma

29 1Nanjing King-friend Biochemical Pharmaceutical

30 3Navinta

31 2PHARMOBEDIENT

32 1Q Pharma Ltd.

33 1Qilu Pharmaceutical

34 2ROTTAPHARM SpA

35 1Ravoos Laboratories

36 2Senores Pharmaceuticals

37 1Somerset Pharmaceuticals Inc

38 1Sun Pharmaceutical Industries Limited

39 1Viatris

40 4Xo Laboratory

41 1Zhejiang Xianju Pharmaceutical Co. Ltd

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

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

04

BPI West
Not Confirmed
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BPI West
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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05

BPI West
Not Confirmed
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BPI West
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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06

BPI West
Not Confirmed
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BPI West
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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07

BPI West
Not Confirmed
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BPI West
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1996-10-28

Application Number : 74540

Regulatory Info : DISCN

Registration Country : USA

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08

BPI West
Not Confirmed
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BPI West
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

BPI West
Not Confirmed
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BPI West
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

BPI West
Not Confirmed
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BPI West
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : CARDENE

Dosage Form : INJECTABLE;INJECTION

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

Packaging :

Approval Date : 1992-01-30

Application Number : 19734

Regulatory Info : RX

Registration Country : USA

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11

BPI West
Not Confirmed
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BPI West
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

BPI West
Not Confirmed
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BPI West
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

BPI West
Not Confirmed
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BPI West
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

BPI West
Not Confirmed
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BPI West
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

BPI West
Not Confirmed
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BPI West
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

BPI West
Not Confirmed
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BPI West
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

BPI West
Not Confirmed
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BPI West
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

BPI West
Not Confirmed
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BPI West
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

BPI West
Not Confirmed
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BPI West
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

BPI West
Not Confirmed
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BPI West
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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