Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
01 1Octavius Pharma Pvt. Ltd
02 1Mankind Pharma
03 1Sichuan Qingmu Pharmaceutical
04 2ACS DOBFAR SPA
05 2ANDA Repository
06 6ANI Pharmaceuticals Inc
07 1Aguettant
08 1American Regent
09 3Amneal Pharmaceuticals
10 1Amospharm
11 2Anwita Drugs
12 1Aurobindo Pharma Limited
13 2Bionpharma
14 10CHIESI USA INC
15 2Caplin Point Laboratories Limited
16 2Cipla
17 1Clinigen Group
18 1Cooper Pharma Limited
19 1Deva Holding AS
20 2Epic Pharma. LLC.
21 4Farbe Firma
22 2Ferrer Internacional
23 2Glenmark Pharmaceuticals
24 1Ha Noi CPC1 Pharmaceutical JSC
25 4Hikma Pharmaceuticals
26 2Kern Pharma S.L.
27 1Micro Labs Limited
28 1Montage Laboratories
29 1Murli Krishna Pharma
30 1NANJING KING FRIEND
31 3Navinta
32 2PHARMOBEDIENT
33 1Q Pharma Ltd.
34 1RK Pharma
35 2ROTTAPHARM SpA
36 1Ravoos Laboratories
37 1Sun Pharmaceutical Industries Limited
38 1Viatris
39 4Xo Laboratory
40 1Zhejiang Xianju Pharmaceutical Co. Ltd
01 3CAPSULE, EXTENDED RELEASE;ORAL
02 22CAPSULE;ORAL
03 2Coated Tablet
04 1Extended-Release Hard Capsule
05 1Hard Capsule
06 1INF
07 13INJECTABLE;INJECTION
08 12INJECTABLE;INTRAVENOUS
09 1Injectable Solution
10 7Injection
11 1Intravenous, Injectable
12 1Liquid Injection
13 1Modified-Release Hard Capsule
14 1Nicardipine 20Mg 50 Combined Oral Use
15 2Nicardipine 40Mg 30 Joined' Oral Use
16 1PELLET
17 1Pellets For Capsule
18 1Pellets for Capsules
19 1SR PELLET
20 1SR Pellets
21 1Solution For Infusion
22 1Solution for Injection
23 3Tablet
01 1Allowed
02 6Authorized
03 3Cancelled
04 17DISCN
05 1Generic
06 1Originator
07 31RX
08 19Blank
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 1Flusemide
10 2Lincil
11 32NICARDIPINE HYDROCHLORIDE
12 1NICARDIPINE HYDROCHLORIDE IN 0.83% SODIUM CHLORIDE
13 1NICARDIPINE HYDROCHLORIDE IN 0.86% SODIUM CHLORIDE
14 6NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE
15 1Nerdipina
16 1Nerdipina Retard
17 1Nicardipin Aguettant
18 3Nicardipine
19 1Nicardipine Equity
20 1Nicardipine Injection
21 3Vasonase
22 1Vasonase Retard
23 11Blank
01 1China
02 11India
03 3Italy
04 1South Africa
05 1South Korea
06 9Spain
07 1Switzerland
08 1Turkey
09 50USA
10 1Vietnam
Octavius Pharma 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
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
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
Qingmu Pharma: Patients first, FDA/CEP/US-DMF/US-VMF/ASMF APIs for Humans & Vets in 100+ countries.
Regulatory Info : RX
Registration Country : USA
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
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 : 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 : 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
