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01 1AbbVie Inc

02 1Biophore India Pharmaceuticals Pvt Ltd

03 1Dr. Reddy's Laboratories

04 1?resund Pharma Aps

05 1ABRAXIS PHARM

06 1Abbott Laboratories

07 1Adcock Ingram

08 1Amneal Pharmaceuticals

09 1Amphastar Pharmaceuticals

10 1Aurobindo Pharma Limited

11 1Avet Pharmaceuticals

12 1Bausch Health

13 1Baxter Healthcare Corporation

14 2Biological E

15 1Caplin Point Laboratories Limited

16 1Chartwell Pharmaceuticals llc

17 1Cipla

18 1DR REDDY'S LABORATORIES LTD

19 1Epic Pharma. LLC.

20 1Etico Lifesciences

21 3Exela Pharma Sciences, LLC.

22 1F. Hoffmann-La Roche

23 4Farbe Firma

24 1Genchain Biotech

25 1Hainan Poly Pharm

26 1Hospira, Inc.

27 1MARCAN PHARMACEUTICALS INC

28 1Micro Labs Limited

29 1Nexus Pharmaceuticals

30 1Oresund Pharma ApS

31 1Ospedalia Ag

32 1PHARMOBEDIENT

33 1Pfizer Inc

34 1STERIMAX INC

35 1Sagent Pharmaceuticals

36 4Slate Run Pharmaceuticals

37 1Solfran Laboratories

38 1Somerset Pharmaceuticals Inc

39 1Sun Pharmaceutical Industries Limited

40 1Teva Pharmaceutical Industries

41 1Urquima S.A. Grupo Uriach

42 2Viatris

43 1Xiromed

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PharmaCompass

01

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Dosage Strength : 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

Fall Technical Meeting
Not Confirmed
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Fall Technical Meeting
Not Confirmed

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

PHARMOBEDIENT

Country
Fall Technical Meeting
Not Confirmed
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PHARMOBEDIENT

Country
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Fall Technical Meeting
Not Confirmed

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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