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 8Baxter 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 1GATOR PHARMS
21 2GLAND PHARMA LIMITED
22 2Genchain Biotech
23 2Grindeks AS
24 6HQ SPCLT PHARMA
25 9Hospira, Inc.
26 1KIVIPharm
27 1Lukare medical
28 3MONICO SpA
29 3Milla Pharmaceuticals
30 1Novel Laboratories, Inc.
31 1PAI HOLDINGS
32 1Perrigo Company plc
33 1Polifarma
34 5SALF SpA
35 1Sandoz B2B
36 1Taro Pharmaceutical Industries
37 1United Biomed
38 2Vefa Ilac
39 1Verve Human Care Laboratories
40 3Viatris
41 1Zuma Pharma
42 1Blank
01 1Ampoule
02 2CAPSULE
03 1Concentrate to the infusion fluid
04 1Concentrate to the infusion fluid, resolution
05 3EMULSION
06 7EMULSION;INTRAVENOUS
07 37INJECTABLE;INJECTION
08 1INJECTABLE;INTRATHECAL
09 2INJECTION
10 1IV Infusion for Solution
11 6Injection
12 2LIQUID
13 1Liquid
14 1POWDER FOR SOLUTION
15 1POWDER;ORAL
16 2SOLUTION
17 2SOLUTION FOR INJECTION
18 7SOLUTION;INTRAMUSCULAR, INTRAVENOUS
19 2SOLUTION;IRRIGATION
20 10SOLUTION;ORAL
21 2Solution For Hemodialysis
22 1TABLET
23 1TABLET;ORAL
24 8Blank
01 3DISCN
02 6Generic
03 1Generic eCTD
04 62RX
05 30Blank
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 INJECTION USP
13 1MAGNESIUM SULFATE INJECTION, BP 49.3%
14 1MAGNESIUM SULFATE INJECTION, USP
15 8Magnesium Sulfate
16 1Magnesium sulphate B. Braun
17 1Mebocit
18 3PERIKABIVEN IN PLASTIC CONTAINER
19 1SMOFKABIVEN
20 1SMOFKABIVEN EXTRA NITROGEN
21 1SMOFKABIVEN PERIPHERAL
22 7SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE
23 1SUCLEAR
24 1SULFAVITE
25 1SUPREP BOWEL PREP KIT
26 1SUTAB
27 1TIS-U-SOL
28 1TIS-U-SOL IN PLASTIC CONTAINER
29 1TIS-U-SOL SOLUTION
30 1VERMAG
31 13Blank
01 1Bahrain
02 2Brazil
03 8Canada
04 3China
05 1Egypt
06 1France
07 2India
08 8Italy
09 2Latvia
10 2Norway
11 3Turkey
12 66USA
13 1Uzbekistan
14 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
