01 1ABBVIE
02 1DR REDDYS
03 1ABBOTT
04 1ABRAXIS PHARM
05 1AMNEAL
06 1AMPHASTAR PHARMS INC
07 1AVET LIFESCIENCES
08 1BAXTER HLTHCARE
09 1BE PHARMS
10 1CAPLIN
11 1CHARTWELL RX
12 1CIPLA
13 1EPIC PHARMA LLC
14 1EUGIA PHARMA
15 3EXELA PHARMA
16 1HOSPIRA
17 1MICRO LABS
18 1MYLAN LABS LTD
19 1NEXUS
20 1NORVIUM BIOSCIENCE
21 1ROCHE
22 1SAGENT PHARMS INC
23 4SLATE RUN PHARMA
24 1SOMERSET THERAPS LLC
25 1SUN PHARM
26 1TEVA PARENTERAL
27 1VPNA
28 1XIROMED
01 27INJECTABLE;INJECTION
02 6SOLUTION;INTRAVENOUS
01 16DISCN
02 17RX
01 1NIPRIDE
02 3NIPRIDE RTU IN SODIUM CHLORIDE 0.9%
03 4NITROPRESS
04 25SODIUM NITROPRUSSIDE
01 28No
02 5Yes
RLD : Yes
TE Code :
Brand Name : NITROPRESS
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 18450
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AP
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Approval Date : 2019-04-10
Application Number : 210114
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code :
Brand Name : NITROPRESS
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/VIAL
Approval Date : 1987-11-16
Application Number : 71555
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/VIAL
Approval Date : 1985-01-17
Application Number : 70031
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : NITROPRESS
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Approval Date : 1988-08-01
Application Number : 71961
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-07-28
Application Number : 18581
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : NIPRIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/VIAL
Approval Date : 1982-01-01
Application Number : 17546
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : NITROPRESS
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/VIAL
Approval Date : 1986-06-09
Application Number : 70566
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AP
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Approval Date : 2016-12-08
Application Number : 207426
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code :
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Approval Date : 1992-03-30
Application Number : 73465
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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