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01 1Ethypharm

02 2Strides Pharma Science

03 1Adcock Ingram

04 1Alkem Laboratories

05 2Amneal Pharmaceuticals

06 1Annora Pharma

07 4Aspiro Pharma

08 2Azurity Pharma

09 4B. Braun Medical

10 1B. Braun Melsungen AG

11 1BRAINTREE LABS

12 1Bahrain Pharma

13 11Baxter Healthcare Corporation

14 1Bionpharma

15 1Bristol Myers Squibb

16 4Central Procurement & Supplies Unit

17 1Cooper Pharma Limited

18 1DOMINION VETERINARY LABORATORIES LTD.

19 2Demo S.A.

20 1Eurofarma Laboratorios S.A

21 1Exela Pharma Sciences, LLC.

22 9Fresenius Kabi AB Brunna

23 4Fresenius Kabi Austria

24 17Fresenius Kabi USA

25 5Fresenius SE & Co. KGaA

26 1GATOR PHARMS

27 2GLAND PHARMA LIMITED

28 2Genchain Biotech

29 6HQ SPCLT PHARMA

30 9Hospira, Inc.

31 1KIVIPharm

32 1LABORATOIRES STEROP NV

33 3Laboratorios ERN

34 1Louis Widmer

35 1Lukare medical

36 3MONICO SpA

37 1Medius Ag

38 3Milla Pharmaceuticals

39 1Mit Health Gmbh

40 2Montage Laboratories

41 1Novel Laboratories, Inc.

42 1PAC3 Limited

43 1PAI HOLDINGS

44 1PHARMOBEDIENT

45 1Perrigo Company plc

46 1Polifarma

47 5SALF SpA

48 1Sandoz B2B

49 1Taro Pharmaceutical Industries

50 1Themis Medicare

51 1United Biomed

52 2Vefa Ilac

53 1Verve Human Care Laboratories

54 2Viatris

55 1Xvivo Perfusion Ab

56 1Zuma Pharma

57 2Blank

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PharmaCompass

01

  • 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

Magnesium Sulfate

Brand Name :

Dosage Form : Ampoule

Dosage Strength : 150MG/1ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : France

Ethypharm

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

Regulatory Info : RX

Registration Country : USA

MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE

Brand Name : SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE

Dosage Form : SOLUTION;ORAL

Dosage Strength : 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT

Packaging :

Approval Date : 2023-11-22

Application Number : 215469

Regulatory Info : RX

Registration Country : USA

Strides Pharma Science

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

Regulatory Info :

Registration Country : India

Sodium Sulfate; Potassium Sulfate; Magnesium Sulfate

Brand Name : Sodium Sulfate; Potassium Sulfate; Magnesium Sulfate

Dosage Form : Oral Solution

Dosage Strength : (17.5 g/3.13 g/1.6 g) per 6 ounces

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

04

AES
Not Confirmed
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MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE

Brand Name : SUPREP BOWEL PREP KIT

Dosage Form : SOLUTION;ORAL

Dosage Strength : 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT

Packaging :

Approval Date : 2010-08-05

Application Number : 22372

Regulatory Info : RX

Registration Country : USA

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05

AES
Not Confirmed
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AES
Not Confirmed

MAGNESIUM SULFATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM PHOSPHATE

Brand Name : TIS-U-SOL IN PLASTIC CONTAINER

Dosage Form : SOLUTION;IRRIGATION

Dosage Strength : 20MG/100ML;40MG/100ML;6.25MG/100ML;800MG/100ML;8.75MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 18336

Regulatory Info : RX

Registration Country : USA

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06

AES
Not Confirmed
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AES
Not Confirmed

MAGNESIUM SULFATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM PHOSPHATE

Brand Name : TIS-U-SOL

Dosage Form : SOLUTION;IRRIGATION

Dosage Strength : 20MG/100ML;40MG/100ML;6.25MG/100ML;800MG/100ML;8.75MG/100ML

Packaging :

Approval Date : 1982-02-19

Application Number : 18508

Regulatory Info : RX

Registration Country : USA

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07

AES
Not Confirmed
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AES
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MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : 5GM/10ML (500MG/ML)

Packaging :

Approval Date : 1986-09-08

Application Number : 19316

Regulatory Info : RX

Registration Country : USA

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08

AES
Not Confirmed
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AES
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MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : 1GM/2ML (500MG/ML)

Packaging :

Approval Date : 1986-09-08

Application Number : 19316

Regulatory Info : RX

Registration Country : USA

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09

AES
Not Confirmed
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AES
Not Confirmed

MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : 10GM/20ML (500MG/ML)

Packaging :

Approval Date : 2016-01-29

Application Number : 19316

Regulatory Info : RX

Registration Country : USA

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10

AES
Not Confirmed
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MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : 25GM/50ML (500MG/ML)

Packaging :

Approval Date : 2016-01-29

Application Number : 19316

Regulatory Info : RX

Registration Country : USA

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11

AES
Not Confirmed
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AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM GLYCEROPHOSPHATE; SOYBEAN OIL

Brand Name : PERIKABIVEN IN PLASTIC CONTAINER

Dosage Form : EMULSION;INTRAVENOUS

Dosage Strength : 2.4%;20MG/100ML;6.8GM/100ML;68MG/100ML;124MG/100ML;170MG/100ML;105MG/100ML;3.5GM/100ML (1440ML)

Packaging :

Approval Date : 2014-08-25

Application Number : 200656

Regulatory Info : RX

Registration Country : USA

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12

AES
Not Confirmed
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AES
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MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 4GM/100ML (40MG/ML)

Packaging :

Approval Date : 1994-06-24

Application Number : 20309

Regulatory Info : RX

Registration Country : USA

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13

AES
Not Confirmed
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AES
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MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 4GM/50ML (80MG/ML)

Packaging :

Approval Date : 1994-06-24

Application Number : 20309

Regulatory Info : RX

Registration Country : USA

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14

AES
Not Confirmed
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AES
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MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 2GM/50ML (40MG/ML)

Packaging :

Approval Date : 2007-01-26

Application Number : 20309

Regulatory Info : RX

Registration Country : USA

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15

AES
Not Confirmed
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AES
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MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20GM/500ML (40MG/ML)

Packaging :

Approval Date : 1995-01-18

Application Number : 20309

Regulatory Info : RX

Registration Country : USA

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16

AES
Not Confirmed
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AES
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MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 40GM/1000ML (40MG/ML)

Packaging :

Approval Date : 1995-01-18

Application Number : 20309

Regulatory Info : RX

Registration Country : USA

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17

AES
Not Confirmed
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AES
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MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE IN DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 1GM/100ML

Packaging :

Approval Date : 1995-07-11

Application Number : 20488

Regulatory Info : RX

Registration Country : USA

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18

AES
Not Confirmed
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MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE IN DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 2GM/100ML

Packaging :

Approval Date : 1995-07-11

Application Number : 20488

Regulatory Info : RX

Registration Country : USA

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19

AES
Not Confirmed
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MAGNESIUM SULFATE

Brand Name : MAGNESIUM SULFATE

Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

Dosage Strength : 5GM/10ML (500MG/ML)

Packaging :

Approval Date : 2000-04-25

Application Number : 75151

Regulatory Info : RX

Registration Country : USA

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20

AES
Not Confirmed
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AES
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

Brand Name : ELLIOTTS B SOLUTION

Dosage Form : INJECTABLE;INTRATHECAL

Dosage Strength : 0.2MG/ML;0.8MG/ML;0.3MG/ML;0.3MG/ML;1.9MG/ML;7.3MG/ML;0.2MG/ML

Packaging :

Approval Date : 1996-09-27

Application Number : 20577

Regulatory Info : RX

Registration Country : USA

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