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01 1Dr. Reddy's Laboratories

02 1Amneal Pharmaceuticals

03 1Aurobindo Pharma Limited

04 1Biological E

05 1Caplin Point Laboratories Limited

06 1Cristalia Produtos Quimicos Farma. Ltda

07 3ENDO OPERATIONS

08 2Exela Pharma Sciences, LLC.

09 1Fresenius Kabi USA

10 1GLAND PHARMA LIMITED

11 2Hikma Pharmaceuticals

12 1Mankind Pharma

13 2Nexus Pharmaceuticals

14 1PROCTER AND GAMBLE

15 1Pfizer Inc

16 1Renew Biopharma

17 1Sagent Pharmaceuticals

18 2Sandoz B2B

19 1Xiromed

20 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

EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2020-10-03

Application Number : 212649

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

02

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2019-10-23

Application Number : 212932

Regulatory Info : RX

Registration Country : USA

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03

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2021-06-14

Application Number : 214579

Regulatory Info : RX

Registration Country : USA

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04

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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Ephedrine Sulfate

Brand Name :

Dosage Form : Vial

Dosage Strength : 50MG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

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05

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2024-07-18

Application Number : 219050

Regulatory Info : RX

Registration Country : USA

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06

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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Ephedrine Sulfate

Brand Name : EFEDRIN

Dosage Form : INJECTION

Dosage Strength : 50MG/ML

Packaging : 100 AMPS X 1 ML

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : Brazil

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07

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : AKOVAZ

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2016-04-29

Application Number : 208289

Regulatory Info : RX

Registration Country : USA

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08

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : AKOVAZ

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 25MG/5ML (5MG/ML)

Packaging :

Approval Date : 2021-08-02

Application Number : 208289

Regulatory Info : RX

Registration Country : USA

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09

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2020-08-04

Application Number : 209646

Regulatory Info : RX

Registration Country : USA

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10

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2022-02-25

Application Number : 216146

Regulatory Info : RX

Registration Country : USA

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11

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2020-12-15

Application Number : 214334

Regulatory Info : RX

Registration Country : USA

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12

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 25MG/5ML (5MG/ML)

Packaging :

Approval Date :

Application Number : 217721

Regulatory Info :

Registration Country : USA

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13

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2022-04-14

Application Number : 216129

Regulatory Info : RX

Registration Country : USA

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14

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EMERPHED

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/10ML (5MG/ML)

Packaging :

Approval Date : 2020-04-17

Application Number : 213407

Regulatory Info : RX

Registration Country : USA

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15

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EMERPHED

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 25MG/5ML (5MG/ML)

Packaging :

Approval Date : 2023-02-28

Application Number : 213407

Regulatory Info : RX

Registration Country : USA

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16

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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Ephedrine Sulphate

Brand Name : Ephedrine Sulphate Injection 50 mg/ml

Dosage Form : INJ

Dosage Strength : 50mg/ml

Packaging : 1X10mg/ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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17

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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Ephedrine Sulphate

Brand Name : Vicks Medinite

Dosage Form : SYR

Dosage Strength : 8mg/30 ml

Packaging : 180X1mg/30 ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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18

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2017-03-01

Application Number : 208609

Regulatory Info : DISCN

Registration Country : USA

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Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2023-03-09

Application Number : 214528

Regulatory Info : RX

Registration Country : USA

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Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2017-08-23

Application Number : 209784

Regulatory Info : RX

Registration Country : USA

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Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE INJECTION USP

Dosage Form : SOLUTION

Dosage Strength : 50MG/ML

Packaging : 10X1ML

Approval Date :

Application Number : 876534

Regulatory Info : Ethical

Registration Country : Canada

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22

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2022-04-21

Application Number : 215825

Regulatory Info : RX

Registration Country : USA

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23

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2023-05-16

Application Number : 217276

Regulatory Info : DISCN

Registration Country : USA

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24

ENDO OPERATIONS

Country
Fi Europe 2024
Not Confirmed
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ENDO OPERATIONS

Country
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Fi Europe 2024
Not Confirmed

EPHEDRINE SULFATE

Brand Name : CORPHEDRA

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/ML (50MG/ML)

Packaging :

Approval Date : 2017-01-27

Application Number : 208943

Regulatory Info : RX

Registration Country : USA

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25

ENDO OPERATIONS

Country
Fi Europe 2024
Not Confirmed
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ENDO OPERATIONS

Country
arrow
Fi Europe 2024
Not Confirmed

EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 50MG/10ML (5MG/ML)

Packaging :

Approval Date : 2020-10-16

Application Number : 213994

Regulatory Info : RX

Registration Country : USA

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26

ENDO OPERATIONS

Country
Fi Europe 2024
Not Confirmed
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ENDO OPERATIONS

Country
arrow
Fi Europe 2024
Not Confirmed

EPHEDRINE SULFATE

Brand Name : EPHEDRINE SULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 25MG/5ML (5MG/ML)

Packaging :

Approval Date : 2022-04-22

Application Number : 213994

Regulatory Info : RX

Registration Country : USA

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