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01 2Dr. Reddy's Laboratories

02 1Breckenridge Pharmaceutical

03 1Ethypharm

04 1Naprod Life Sciences

05 1Mankind Pharma

06 1ADAPTIS

07 1AMN Life Science

08 1Accord healthcare

09 1Amino AG

10 1Amneal Pharmaceuticals

11 2Amphastar Pharmaceuticals

12 1Amring Pharma

13 1Aspiro Pharma

14 1Aurobindo Pharma Limited

15 1Baxter Healthcare Corporation

16 1Biolik Pharma

17 2Biological E

18 2Bristol Myers Squibb

19 1DR REDDY'S LABORATORIES LTD

20 1Deva Holding AS

21 4Farbe Firma

22 2Flagship Biotech International Pvt. Ltd

23 3Fresenius Kabi USA

24 1Fresenius SE & Co. KGaA

25 1GLAND PHARMA LIMITED

26 1GSK

27 3Hikma Pharmaceuticals

28 4Hospira, Inc.

29 1Meda AB

30 1Meitheal Pharmaceuticals

31 1Merck & Co

32 1Micro Labs Limited

33 1Montage Laboratories

34 1Nexus Pharmaceuticals

35 1Pfizer Inc

36 1Pharma-Q Holdings (Pty) Ltd

37 1Pluviaendo

38 1Sagent Pharmaceuticals

39 4Sandoz B2B

40 1Somerset Pharmaceuticals Inc

41 1Steriscience

42 1Takeda Pharmaceutical

43 1Umedica Laboratories

44 1Xian Libang Pharmaceutical Co.,Ltd

45 1Zydus Pharmaceuticals

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PharmaCompass

01

  • 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

SUCCINYLCHOLINE CHLORIDE

Brand Name : SUCCINYLCHOLINE CHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML

Packaging :

Approval Date : 2019-08-02

Application Number : 210698

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

02

SUCCINYLCHOLINE CHLORIDE

Brand Name : SUCCINYLCHOLINE CHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML

Packaging :

Approval Date : 2019-10-09

Application Number : 212638

Regulatory Info : DISCN

Registration Country : USA

Breckenridge Pharmaceutical

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEthypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.

Regulatory Info :

Registration Country : France

Succinylcholine Chloride

Brand Name :

Dosage Form : Ampoule

Dosage Strength : 50MG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : France

Ethypharm

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Succinylcholine Chloride

Brand Name :

Dosage Form : Liquid Injection

Dosage Strength : 50MG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

05

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

SUCCINYLCHOLINE CHLORIDE

Brand Name : SUCCINYLCHOLINE CHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML

Packaging :

Approval Date : 2023-02-02

Application Number : 216127

Regulatory Info : DISCN

Registration Country : USA

Company Banner

06

  • 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

SUCCINYLCHOLINE CHLORIDE

Brand Name : SUCCINYLCHOLINE CHLORIDE

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : 100MG/5ML (20MG/ML)

Packaging :

Approval Date : 2024-01-17

Application Number : 218467

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

07

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : SUCCINYLCHOLINE CHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/VIAL

Packaging :

Approval Date : 1982-02-04

Application Number : 85400

Regulatory Info : DISCN

Registration Country : USA

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08

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : SUCCINYLCHOLINE CHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML

Packaging :

Approval Date : 2018-06-04

Application Number : 210231

Regulatory Info : RX

Registration Country : USA

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09

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : SUCOSTRIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 8847

Regulatory Info : DISCN

Registration Country : USA

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10

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : SUCOSTRIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 8847

Regulatory Info : DISCN

Registration Country : USA

blank

11

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : QUELICIN PRESERVATIVE FREE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 8845

Regulatory Info : DISCN

Registration Country : USA

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12

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : QUELICIN PRESERVATIVE FREE

Dosage Form : INJECTABLE;INJECTION

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

Packaging :

Approval Date : 1982-01-01

Application Number : 8845

Regulatory Info : DISCN

Registration Country : USA

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13

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : QUELICIN PRESERVATIVE FREE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 8845

Regulatory Info : DISCN

Registration Country : USA

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14

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : QUELICIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 8845

Regulatory Info : RX

Registration Country : USA

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15

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : SUCCINYLCHOLINE CHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 80997

Regulatory Info : DISCN

Registration Country : USA

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16

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : ANECTINE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 500MG/VIAL

Packaging :

Approval Date : 1982-01-01

Application Number : 8453

Regulatory Info : DISCN

Registration Country : USA

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17

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : ANECTINE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 8453

Regulatory Info : RX

Registration Country : USA

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18

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : ANECTINE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 8453

Regulatory Info : DISCN

Registration Country : USA

blank

19

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : ANECTINE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 1GM/VIAL

Packaging :

Approval Date : 1982-01-01

Application Number : 8453

Regulatory Info : DISCN

Registration Country : USA

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20

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

SUCCINYLCHOLINE CHLORIDE

Brand Name : SUCCINYLCHOLINE CHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML

Packaging :

Approval Date : 2018-05-04

Application Number : 209467

Regulatory Info : RX

Registration Country : USA

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