Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
01 1MANKIND PHARMA
02 1CHENGDU SHUODE
03 1AM REGENT
04 3AMNEAL
05 2ANDA REPOSITORY
06 6ANI PHARMS
07 2BIONPHARMA
08 2CAPLIN
09 10CHIESI
10 2CIPLA
11 2EPIC PHARMA LLC
12 1EUGIA PHARMA
13 2GLENMARK PHARMS LTD
14 1HIKMA
15 3HIKMA INTL PHARMS
16 2INFORLIFE
17 1MICRO LABS
18 1NANJING KING FRIEND
19 3NAVINTA LLC
20 2PHARMOBEDIENT
21 1RK PHARMA
22 1SUN PHARM
01 3CAPSULE, EXTENDED RELEASE;ORAL
02 22CAPSULE;ORAL
03 13INJECTABLE;INJECTION
04 12INJECTABLE;INTRAVENOUS
01 17DISCN
02 31RX
03 2Blank
01 3CARDENE
02 1CARDENE IN 0.83% SODIUM CHLORIDE IN PLASTIC CONTAINER
03 1CARDENE IN 0.86% SODIUM CHLORIDE IN PLASTIC CONTAINER
04 1CARDENE IN 4.8% DEXTROSE IN PLASTIC CONTAINER
05 1CARDENE IN 5.0% DEXTROSE IN PLASTIC CONTAINER
06 3CARDENE SR
07 32NICARDIPINE HYDROCHLORIDE
08 1NICARDIPINE HYDROCHLORIDE IN 0.83% SODIUM CHLORIDE
09 1NICARDIPINE HYDROCHLORIDE IN 0.86% SODIUM CHLORIDE
10 6NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE
01 35No
02 13Yes
03 2Blank
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AP
Brand Name : NICARDIPINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/10ML (2.5MG/ML)
Approval Date : 2009-11-17
Application Number : 90671
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
Qingmu Pharma: Patients first, FDA/CEP/US-DMF/US-VMF/ASMF APIs for Humans & Vets in 100+ countries.
RLD : No
TE Code : AP
Brand Name : NICARDIPINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/10ML (2.5MG/ML)
Approval Date : 2024-09-06
Application Number : 217548
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : Yes
TE Code :
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Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1988-12-21
Application Number : 19488
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1988-12-21
Application Number : 19488
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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**
Approval Date : 1992-01-30
Application Number : 19734
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : CARDENE IN 4.8% DEXTROSE IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INTRAVENOUS
Dosage Strength : 20MG/200ML (0.1MG/ML)
Approval Date : 2008-07-31
Application Number : 19734
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code : AP
Brand Name : CARDENE IN 0.86% SODIUM CHLORIDE IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INTRAVENOUS
Dosage Strength : 20MG/200ML (0.1MG/ML)
Approval Date : 2008-07-31
Application Number : 19734
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code : AP
Brand Name : CARDENE IN 0.83% SODIUM CHLORIDE IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INTRAVENOUS
Dosage Strength : 40MG/200ML (0.2MG/ML)
Approval Date : 2008-11-07
Application Number : 19734
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code :
Brand Name : CARDENE IN 5.0% DEXTROSE IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INTRAVENOUS
Dosage Strength : 40MG/200ML (0.2MG/ML)
Approval Date : 2008-11-07
Application Number : 19734
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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**
Approval Date : 1992-02-21
Application Number : 20005
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
