01 1AbbVie Inc
02 1Biophore India Pharmaceuticals Pvt Ltd
03 1Dr. Reddy's Laboratories
04 1ABRAXIS PHARM
05 1Abbott Laboratories
06 1Adcock Ingram
07 1Amneal Pharmaceuticals
08 1Amphastar Pharmaceuticals
09 1Aurobindo Pharma Limited
10 1Avet Pharmaceuticals
11 1Bausch Health
12 1Baxter Healthcare Corporation
13 2Biological E
14 1Caplin Point Laboratories Limited
15 1Chartwell Pharmaceuticals llc
16 1Cipla
17 1DR REDDY'S LABORATORIES LTD
18 1Epic Pharma. LLC.
19 1Etico Lifesciences
20 3Exela Pharma Sciences, LLC.
21 1F. Hoffmann-La Roche
22 4Farbe Firma
23 1Genchain Biotech
24 1Hainan Poly Pharm
25 1Hospira, Inc.
26 1MARCAN PHARMACEUTICALS INC
27 1Micro Labs Limited
28 1NORVIUM BIOSCIENCE
29 1Nexus Pharmaceuticals
30 1Oresund Pharma ApS
31 1Pfizer Inc
32 1STERIMAX INC
33 1Sagent Pharmaceuticals
34 4Slate Run Pharmaceuticals
35 1Solfran Laboratories
36 1Somerset Pharmaceuticals Inc
37 1Sun Pharmaceutical Industries Limited
38 1Teva Pharmaceutical Industries
39 1Viatris
40 1Xiromed
01 1INJ
02 27INJECTABLE;INJECTION
03 1Injectable Injection
04 8Injection
05 1Powder for infusion, solution
06 4SOLUTION
07 6SOLUTION;INTRAVENOUS
08 1Vial
01 16DISCN
02 1Generic
03 4Prescription
04 17RX
05 11Blank
01 1Hypoten L
02 2NIPRIDE
03 3NIPRIDE RTU IN SODIUM CHLORIDE 0.9%
04 4NITROPRESS
05 1Niperum
06 1Nipruss
07 25SODIUM NITROPRUSSIDE
08 3SODIUM NITROPRUSSIDE FOR INJECTION
09 9Blank
01 4Canada
02 2China
03 7India
04 1Mexico
05 1Norway
06 1South Africa
07 33USA
Regulatory Info : DISCN
Registration Country : USA
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Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 18450
Regulatory Info : DISCN
Registration Country : USA
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 25MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2019-04-10
Application Number : 210114
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NITROPRESS
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/VIAL
Packaging :
Approval Date : 1987-11-16
Application Number : 71555
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/VIAL
Packaging :
Approval Date : 1985-01-17
Application Number : 70031
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2017-11-07
Application Number : 209493
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2017-12-18
Application Number : 209832
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2020-12-10
Application Number : 211934
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2022-11-08
Application Number : 208923
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NITROPRESS
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 1988-08-01
Application Number : 71961
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1982-07-28
Application Number : 18581
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2019-11-29
Application Number : 211016
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2018-06-26
Application Number : 209834
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2018-07-16
Application Number : 210855
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2017-05-04
Application Number : 208635
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NIPRIDE RTU IN SODIUM CHLORIDE 0.9%
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 50MG/100ML (0.5MG/ML)
Packaging :
Approval Date : 2017-03-08
Application Number : 209387
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NIPRIDE RTU IN SODIUM CHLORIDE 0.9%
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 10MG/50ML (0.2MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2017-12-07
Application Number : 209387
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NIPRIDE RTU IN SODIUM CHLORIDE 0.9%
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 20MG/100ML (0.2MG/ML)
Packaging :
Approval Date : 2018-07-13
Application Number : 209387
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NIPRIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 17546
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NITROPRESS
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/VIAL
Packaging :
Approval Date : 1986-06-09
Application Number : 70566
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2017-12-08
Application Number : 209352
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2017-05-25
Application Number : 207499
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2016-12-08
Application Number : 207426
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2020-08-25
Application Number : 214199
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2018-08-17
Application Number : 210882
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2018-11-26
Application Number : 210467
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 1992-03-30
Application Number : 73465
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2018-04-17
Application Number : 210763
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2020-10-29
Application Number : 211277
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SODIUM NITROPRUSSIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2018-08-10
Application Number : 209584
Regulatory Info : RX
Registration Country : USA
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