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01 1Octavius Pharma Pvt. Ltd

02 2ACS DOBFAR SPA

03 6ANI Pharmaceuticals Inc

04 1American Regent

05 2Anwita Drugs & Chemicals Pvt Ltd

06 1Aurobindo Pharma Limited

07 2Bionpharma

08 10CHIESI USA INC

09 2Cipla

10 1Cooper Pharma Limited

11 1Deva Holding AS

12 2Epic Pharma. LLC.

13 4Farbe Firma

14 2Glenmark Pharmaceuticals

15 1Ha Noi CPC1 Pharmaceutical JSC

16 3Hikma Pharmaceuticals

17 1Micro Labs Limited

18 2NORVIUM BIOSCIENCE

19 1Navinta

20 1RK Pharma

21 2ROTTAPHARM SpA

22 2SKG-Pharma

23 2Senores Pharmaceuticals

24 1Sichuan Qingmu Pharmaceutical

25 1Sun Pharmaceutical Industries Limited

26 1Viatris

27 1West-ward Pharmaceutical Corp

28 1Wockhardt

29 1Zhejiang Xianju Pharmaceutical Co. Ltd

30 2Blank

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : India

Nicardipine

Brand Name :

Dosage Form : Pellets for Capsule

Dosage Strength : 22%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

02

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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03

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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04

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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05

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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06

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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07

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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08

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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09

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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10

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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11

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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12

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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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13

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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14

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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15

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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16

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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17

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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18

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
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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19

NORVIUM BIOSCIENCE

Country
euroPLX 86 Munich
Not Confirmed
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NORVIUM BIOSCIENCE

Country
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euroPLX 86 Munich
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 1996-07-18

Application Number : 74642

Regulatory Info : DISCN

Registration Country : USA

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20

NORVIUM BIOSCIENCE

Country
euroPLX 86 Munich
Not Confirmed
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NORVIUM BIOSCIENCE

Country
arrow
euroPLX 86 Munich
Not Confirmed

NICARDIPINE HYDROCHLORIDE

Brand Name : NICARDIPINE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1996-07-18

Application Number : 74642

Regulatory Info : DISCN

Registration Country : USA

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