Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
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01 1Octavius Pharma Pvt. Ltd
02 2ACS DOBFAR SPA
03 6ANI Pharmaceuticals Inc
04 1American Regent
05 1Amneal Pharmaceuticals
06 2Anwita Drugs
07 1Aurobindo Pharma Limited
08 2Bionpharma
09 10CHIESI USA INC
10 2Cipla
11 1Clinigen Group
12 1Cooper Pharma Limited
13 1Deva Holding AS
14 2Epic Pharma. LLC.
15 4Farbe Firma
16 2Glenmark Pharmaceuticals
17 1Ha Noi CPC1 Pharmaceutical JSC
18 4Hikma Pharmaceuticals
19 1Loxim Industries
20 1Micro Labs Limited
21 1Murli Krishna Pharma
22 2NORVIUM BIOSCIENCE
23 1Navinta
24 1RK Pharma
25 2ROTTAPHARM SpA
26 2SKG-Pharma
27 2Senores Pharmaceuticals
28 1Sichuan Qingmu Pharmaceutical
29 1Sun Pharmaceutical Industries Limited
30 1Viatris
31 1Wockhardt
32 1Zhejiang Xianju Pharmaceutical Co. Ltd
33 2Blank
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01 3CAPSULE, EXTENDED RELEASE;ORAL
02 20CAPSULE;ORAL
03 1INF
04 12INJECTABLE;INJECTION
05 10INJECTABLE;INTRAVENOUS
06 6Injection
07 1Intravenous, Injectable
08 2Modified Release Capsule
09 1Nicardipine 20Mg 50 Combined Oral Use
10 2Nicardipine 40Mg 30 Joined' Oral Use
11 1PELLET
12 1Pellets For Capsule
13 1Pellets for Capsules
14 1Pellets for capsules
15 1SR PELLET
16 1Solution for Injection
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01 17DISCN
02 1Generic
03 1Originator
04 28RX
05 17Blank
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01 1BFS-Nicardipin
02 2Bionicard
03 3CARDENE
04 1CARDENE IN 0.83% SODIUM CHLORIDE IN PLASTIC CONTAINER
05 1CARDENE IN 0.86% SODIUM CHLORIDE IN PLASTIC CONTAINER
06 1CARDENE IN 4.8% DEXTROSE IN PLASTIC CONTAINER
07 1CARDENE IN 5.0% DEXTROSE IN PLASTIC CONTAINER
08 3CARDENE SR
09 29NICARDIPINE HYDROCHLORIDE
10 1NICARDIPINE HYDROCHLORIDE IN 0.83% SODIUM CHLORIDE
11 1NICARDIPINE HYDROCHLORIDE IN 0.86% SODIUM CHLORIDE
12 4NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE
13 1Nerdipina Retard 40Mg 60 Capsules
14 1Nicardipin Retard 40Mg 60 Capsules
15 2Nicardipine
16 1Nicardipine Equity
17 11Blank
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01 1China
02 10India
03 3Italy
04 1South Africa
05 2Spain
06 1Turkey
07 45USA
08 1Vietnam
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Brand Name : Nicardipine
Dosage Form : Pellets for Capsules
Dosage Strength : 22%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
Brand Name : NICARDIPINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/10ML (2.5MG/ML)
Packaging :
Approval Date : 2009-11-17
Application Number : 90534
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
Brand Name : NICARDIPINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 20MG
Packaging :
Approval Date : 1996-10-28
Application Number : 74670
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NICARDIPINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Packaging :
Approval Date : 1996-10-28
Application Number : 74670
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
Brand Name : NICARDIPINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 20MG
Packaging :
Approval Date : 1998-03-19
Application Number : 74928
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NICARDIPINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Packaging :
Approval Date : 1998-03-19
Application Number : 74928
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NICARDIPINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/10ML (2.5MG/ML)
Packaging :
Approval Date : 2009-12-28
Application Number : 78714
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NICARDIPINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/10ML (2.5MG/ML)
Packaging :
Approval Date : 2009-11-17
Application Number : 90125
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NICARDIPINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/10ML (2.5MG/ML)
Packaging :
Approval Date : 2009-11-17
Application Number : 90664
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NICARDIPINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/10ML (2.5MG/ML)
Packaging :
Approval Date : 2009-11-17
Application Number : 78405
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
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
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF