Ethypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.
01 1Ethypharm
02 1Strides Pharma Science
03 1Alkem Laboratories
04 2Amneal Pharmaceuticals
05 1Annora Pharma
06 4B. Braun Medical
07 1B. Braun Melsungen AG
08 3BRAINTREE LABS
09 1Bahrain Pharma
10 9Baxter Healthcare Corporation
11 1Bionpharma
12 1Cooper Pharma Limited
13 1DOMINION VETERINARY LABORATORIES LTD.
14 2Demo S.A.
15 1Eurofarma Laboratorios S.A
16 1Exela Pharma Sciences, LLC.
17 1Fresenius Kabi AB Brunna
18 4Fresenius Kabi Austria
19 17Fresenius Kabi USA
20 5Fresenius SE & Co. KGaA
21 1GATOR PHARMS
22 2GLAND PHARMA LIMITED
23 2Genchain Biotech
24 2Grindeks AS
25 6HQ SPCLT PHARMA
26 9Hospira, Inc.
27 1KIVIPharm
28 1Lukare medical
29 3MONICO SpA
30 3Milla Pharmaceuticals
31 1NORVIUM BIOSCIENCE
32 1Novel Laboratories, Inc.
33 1PAI HOLDINGS
34 1Perrigo Company plc
35 1Polifarma
36 5SALF SpA
37 1Sandoz B2B
38 1Taro Pharmaceutical Industries
39 1United Biomed
40 2Vefa Ilac
41 1Verve Human Care Laboratories
42 2Viatris
43 1Zuma Pharma
44 1Blank
01 1Ampoule
02 2CAPSULE
03 1Concentrate to the infusion fluid
04 1Concentrate to the infusion fluid, resolution
05 3EMULSION
06 7EMULSION;INTRAVENOUS
07 5INF
08 37INJECTABLE;INJECTION
09 1INJECTABLE;INTRATHECAL
10 2INJECTION
11 1IV Infusion for Solution
12 6Injection
13 2LIQUID
14 1Liquid
15 1POWDER FOR SOLUTION
16 1POWDER;ORAL
17 3SOLUTION
18 2SOLUTION FOR INJECTION
19 7SOLUTION;INTRAMUSCULAR, INTRAVENOUS
20 2SOLUTION;IRRIGATION
21 10SOLUTION;ORAL
22 2Solution For Hemodialysis
23 1TABLET
24 1TABLET;ORAL
25 8Blank
01 3DISCN
02 8Ethical
03 7Generic
04 1Generic eCTD
05 4Originator
06 1Prescription
07 62RX
08 22Blank
01 1Addex-Magnesium
02 1Arteasy
03 1COLPREP KIT
04 1ELLIOTTS B SOLUTION
05 1Eurofar
06 1Intertonic Liquid
07 4KABIVEN IN PLASTIC CONTAINER
08 10MAGNESIUM SULFATE
09 1MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE
10 7MAGNESIUM SULFATE IN DEXTROSE 5% IN PLASTIC CONTAINER
11 27MAGNESIUM SULFATE IN PLASTIC CONTAINER
12 1MAGNESIUM SULFATE IN WATER FOR INJECTION
13 1MAGNESIUM SULFATE INJECTION USP
14 1MAGNESIUM SULFATE INJECTION, BP 49.3%
15 1MAGNESIUM SULFATE INJECTION, USP
16 8Magnesium Sulfate
17 1Magnesium sulphate B. Braun
18 1Mebocit
19 3PERIKABIVEN IN PLASTIC CONTAINER
20 5SMOFKABIVEN
21 1SMOFKABIVEN EXTRA NITROGEN
22 2SMOFKABIVEN PERIPHERAL
23 7SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE
24 1SUCLEAR
25 1SULFAVITE
26 1SUPREP BOWEL PREP KIT
27 1SUTAB
28 1TIS-U-SOL
29 1TIS-U-SOL IN PLASTIC CONTAINER
30 1TIS-U-SOL SOLUTION
31 1VERMAG
32 13Blank
01 1Bahrain
02 2Brazil
03 9Canada
04 3China
05 1Egypt
06 1France
07 2India
08 8Italy
09 2Latvia
10 2Norway
11 5South Africa
12 3Turkey
13 66USA
14 1Uzbekistan
15 2Blank
Ethypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.
Regulatory Info :
Registration Country : France
Brand Name :
Dosage Form : Ampoule
Dosage Strength : 150MG/1ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
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 : 2024-06-24
Application Number : 204135
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
MAGNESIUM SULFATE; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; POTASSIUM SULFATE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE
Brand Name : SUCLEAR
Dosage Form : SOLUTION;ORAL
Dosage Strength : 1.6GM/BOT,3.13GM/BOT,17.5GM/BOT,N/A,N/A,N/A,N/A;N/A,N/A,N/A,210GM,0.74GM,2.86GM,5.6GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reason
Packaging :
Approval Date : 2013-01-18
Application Number : 203595
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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 (1920ML)
Packaging :
Approval Date : 2014-08-25
Application Number : 200656
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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 (2400ML)
Packaging :
Approval Date : 2014-08-25
Application Number : 200656
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM GLYCEROPHOSPHATE; SOYBEAN OIL
Brand Name : KABIVEN IN PLASTIC CONTAINER
Dosage Form : EMULSION;INTRAVENOUS
Dosage Strength : 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML ;147MG/100ML;3.9GM/100ML (1026ML)
Packaging :
Approval Date : 2014-08-25
Application Number : 200656
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM GLYCEROPHOSPHATE; SOYBEAN OIL
Brand Name : KABIVEN IN PLASTIC CONTAINER
Dosage Form : EMULSION;INTRAVENOUS
Dosage Strength : 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML;147MG/100ML;3.9GM/100ML (1540ML)
Packaging :
Approval Date : 2014-08-25
Application Number : 200656
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM GLYCEROPHOSPHATE; SOYBEAN OIL
Brand Name : KABIVEN IN PLASTIC CONTAINER
Dosage Form : EMULSION;INTRAVENOUS
Dosage Strength : 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML;147MG/100ML;3.9GM/100ML (2053ML)
Packaging :
Approval Date : 2014-08-25
Application Number : 200656
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM GLYCEROPHOSPHATE; SOYBEAN OIL
Brand Name : KABIVEN IN PLASTIC CONTAINER
Dosage Form : EMULSION;INTRAVENOUS
Dosage Strength : 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML;147MG/100ML;3.9GM/100ML (2566ML)
Packaging :
Approval Date : 2014-08-25
Application Number : 200656
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
Brand Name : MAGNESIUM SULFATE
Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS
Dosage Strength : 10GM/20ML (500MG/ML)
Packaging :
Approval Date : 2015-05-14
Application Number : 202411
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
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 : 2017-02-23
Application Number : 202511
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : USA
MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE
Brand Name : MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : 1.6GM/BOT; 3.13GM/BOT; 17.5GM/BOT
Packaging :
Approval Date :
Application Number : 203102
Regulatory Info :
Registration Country : USA
