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 1AMNEAL
05 6ANI PHARMS
06 2BIONPHARMA
07 10CHIESI
08 2CIPLA
09 2EPIC PHARMA LLC
10 1EUGIA PHARMA
11 2GLENMARK PHARMS LTD
12 1HIKMA
13 3HIKMA INTL PHARMS
14 2INFORLIFE
15 1MICRO LABS
16 3NAVINTA LLC
17 2NORVIUM BIOSCIENCE
18 1RK PHARMA
19 2SENORES PHARMS
20 2SKG PHARMA
21 1SUN PHARM
01 3CAPSULE, EXTENDED RELEASE;ORAL
02 22CAPSULE;ORAL
03 12INJECTABLE;INJECTION
04 10INJECTABLE;INTRAVENOUS
01 17DISCN
02 30RX
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 31NICARDIPINE HYDROCHLORIDE
08 1NICARDIPINE HYDROCHLORIDE IN 0.83% SODIUM CHLORIDE
09 1NICARDIPINE HYDROCHLORIDE IN 0.86% SODIUM CHLORIDE
10 4NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE
01 34No
02 13Yes
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
Sichuan Qingmu Pharmaceutical offers reliable CDMO support and high-quality APIs for regulated markets.
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Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
