Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

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01 1MANKIND PHARMA
02 1CHENGDU SHUODE
03 1AM REGENT
04 3AMNEAL
05 6ANI PHARMS
06 2BIONPHARMA
07 2CAPLIN
08 10CHIESI
09 2CIPLA
10 2EPIC PHARMA LLC
11 1EUGIA PHARMA
12 2GLENMARK PHARMS LTD
13 1HIKMA
14 3HIKMA INTL PHARMS
15 2INFORLIFE
16 1MICRO LABS
17 1NANJING KING FRIEND
18 3NAVINTA LLC
19 2PHARMOBEDIENT
20 1QILU PHARM HAINAN
21 2SENORES PHARMS
22 1SOMERSET THERAPS LLC
23 1SUN PHARM
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01 3CAPSULE, EXTENDED RELEASE;ORAL
02 22CAPSULE;ORAL
03 14INJECTABLE;INJECTION
04 12INJECTABLE;INTRAVENOUS
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01 16DISCN
02 35RX
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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 33NICARDIPINE 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 38No
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
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
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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Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :

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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Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :

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RLD : Yes
TE Code : AP
Brand Name : CARDENE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/10ML (2.5MG/ML)
Approval Date : 1992-01-30
Application Number : 19734
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP

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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 :

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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

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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

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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 :

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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 :
