Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
01 1Octavius Pharma Pvt. Ltd
02 2ACS DOBFAR SPA
03 6ANI Pharmaceuticals Inc
04 1American Regent
05 1Amneal Pharmaceuticals
06 2Anwita Drugs & Chemicals Pvt Ltd
07 1Aurobindo Pharma Limited
08 2Bionpharma
09 10CHIESI USA INC
10 2Cipla
11 1Cooper Pharma Limited
12 1Deva Holding AS
13 2Epic Pharma. LLC.
14 4Farbe Firma
15 2Glenmark Pharmaceuticals
16 1Ha Noi CPC1 Pharmaceutical JSC
17 3Hikma Pharmaceuticals
18 1Micro Labs Limited
19 2NORVIUM BIOSCIENCE
20 1Navinta
21 1RK Pharma
22 2ROTTAPHARM SpA
23 2SKG-Pharma
24 2Senores Pharmaceuticals
25 1Sichuan Qingmu Pharmaceutical
26 1Sun Pharmaceutical Industries Limited
27 1Viatris
28 1West-ward Pharmaceutical Corp
29 1Wockhardt
30 1Zhejiang Xianju Pharmaceutical Co. Ltd
31 2Blank
01 3CAPSULE, EXTENDED RELEASE;ORAL
02 20CAPSULE;ORAL
03 12INJECTABLE;INJECTION
04 10INJECTABLE;INTRAVENOUS
05 6Injection
06 1Intravenous, Injectable
07 2Modified Release Capsule
08 1Nicardipine 20Mg 50 Combined Oral Use
09 2Nicardipine 40Mg 30 Joined' Oral Use
10 1Pellets for Capsule
11 2SR Pellet
12 1Solution for Injection
01 16DISCN
02 1Generic
03 29RX
04 15Blank
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 1Nicardipine
16 10Blank
01 1China
02 8India
03 3Italy
04 2Spain
05 1Turkey
06 45USA
07 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 :
Dosage Form : Pellets for Capsule
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 : 2009-11-17
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 : 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 : 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
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