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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

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PharmaCompass

01

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SODIUM NITROPRUSSIDE

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Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

Abbvie Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothBiophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

Regulatory Info :

Registration Country : India

Sodium Nitroprusside

Brand Name :

Dosage Form : Injection

Dosage Strength : 25MG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Biophore

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

SODIUM NITROPRUSSIDE

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

Dr Reddy Company Banner

04

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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05

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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06

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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07

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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08

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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09

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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10

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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11

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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12

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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13

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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14

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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15

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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16

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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17

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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18

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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19

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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

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20

NORVIUM BIOSCIENCE

Country
2024 ACI Convention
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NORVIUM BIOSCIENCE

Country
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2024 ACI Convention
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SODIUM NITROPRUSSIDE

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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