01 22Adcock Ingram
02 3Baxter Healthcare Corporation
03 1Fresenius Kabi AB Brunna
04 3Fresenius Kabi Austria
05 7Fresenius Kabi USA
06 5Fresenius SE & Co. KGaA
07 1SIT LABORATORIO FARMAC. Srl
08 1TEOFARMA Srl
01 1CONCENTRATE FOR SOLUTION FOR INFUSION
02 6EMULSION
03 7EMULSION;INTRAVENOUS
04 26INF
05 1SOL
06 2Blank
01 6Ethical
02 1Generic
03 26Originator
04 7RX
05 3Blank
01 1Extraneal
02 1Glicerovalerovit
03 1Glycophos
04 4KABIVEN IN PLASTIC CONTAINER
05 1Neurol
06 1OLIMEL 5.7% E
07 1OLIMEL 7.6% E
08 1Oliclinomel N4-550 E
09 2Oliclinomel N6-900 E
10 1Oliclinomel N7-1000 E
11 3PERIKABIVEN IN PLASTIC CONTAINER
12 1PERIOLIMEL 2.5% E
13 5SMOFKABIVEN
14 1SMOFKABIVEN EXTRA NITROGEN
15 2SMOFKABIVEN PERIPHERAL
16 1Sabax Ciprofloxacin 2Mg/Ml (50Ml)
17 6TRIOMEL N4-600E
18 4TRIOMEL N7-960E
19 6TRIOMEL N9-840 E
01 6Canada
02 2Italy
03 27South Africa
04 1Sweden
05 7USA
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Extraneal
Dosage Form : SOL
Dosage Strength : 75g/1000ml
Packaging : 2000X1g/1000ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Oliclinomel N4-550 E
Dosage Form : INF
Dosage Strength : 100g/1000ml
Packaging : 2500X1%/bag
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Oliclinomel N6-900 E
Dosage Form : INF
Dosage Strength : 100g/1000ml
Packaging : 2000X4%/bag
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Oliclinomel N6-900 E
Dosage Form : INF
Dosage Strength : 200g/1000ml
Packaging : 2000X1%/bag
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Oliclinomel N7-1000 E
Dosage Form : INF
Dosage Strength : 5g/1000ml
Packaging : 2000X1%/bag
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Sabax Ciprofloxacin 2Mg/Ml (50Ml)
Dosage Form : INF
Dosage Strength : 2mg/ml
Packaging : 50X1mg/ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : TRIOMEL N4-600E
Dosage Form : INF
Dosage Strength : 30g/1000ml
Packaging : 1000X1g/1000ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : TRIOMEL N4-600E
Dosage Form : INF
Dosage Strength : 30g/1000ml
Packaging : 1000X1g/1000ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : TRIOMEL N4-600E
Dosage Form : INF
Dosage Strength : 30g/1000ml
Packaging : 1500X1g/1000ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : TRIOMEL N4-600E
Dosage Form : INF
Dosage Strength : 30g/1000ml
Packaging : 1500X1g/1000ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : TRIOMEL N7-960E
Dosage Form : INF
Dosage Strength : 140g/1000ml
Packaging : 1000X1g/1000ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : TRIOMEL N7-960E
Dosage Form : INF
Dosage Strength : 40g/1000ml
Packaging : 1000X1g/1000ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : TRIOMEL N7-960E
Dosage Form : INF
Dosage Strength : 140g/1000ml
Packaging : 2000X1g/1000ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : TRIOMEL N7-960E
Dosage Form : INF
Dosage Strength : 40g/1000ml
Packaging : 2000X1g/1000ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Ethical
Registration Country : Canada
Brand Name : PERIOLIMEL 2.5% E
Dosage Form : EMULSION
Dosage Strength : 1.91G/L
Packaging : 1000/1500/2000/2500ML
Approval Date :
Application Number : 2352494
Regulatory Info : Ethical
Registration Country : Canada
Regulatory Info : Ethical
Registration Country : Canada
Brand Name : OLIMEL 5.7% E
Dosage Form : EMULSION
Dosage Strength : 3.67G/L
Packaging : 1000/1500/2000/2500ML
Approval Date :
Application Number : 2352532
Regulatory Info : Ethical
Registration Country : Canada
Regulatory Info : Ethical
Registration Country : Canada
Brand Name : OLIMEL 7.6% E
Dosage Form : EMULSION
Dosage Strength : 3.67G/L
Packaging : 650/1000/1500/2000ML
Approval Date :
Application Number : 2477955
Regulatory Info : Ethical
Registration Country : Canada
Regulatory Info :
Registration Country : Sweden
sodium glycerophosphate, hydrated
Brand Name : Glycophos
Dosage Form : CONCENTRATE FOR SOLUTION FOR INFUSION
Dosage Strength : -
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info : Ethical
Registration Country : Canada
Brand Name : SMOFKABIVEN
Dosage Form : EMULSION
Dosage Strength : 0.21G/100ML
Packaging : 986/1477/1970/2463ML
Approval Date :
Application Number : 2440695
Regulatory Info : Ethical
Registration Country : Canada
Regulatory Info : Ethical
Registration Country : Canada
Brand Name : SMOFKABIVEN PERIPHERAL
Dosage Form : EMULSION
Dosage Strength : 130MG/100ML
Packaging : 4X1206/4X1448/4X1904ML
Approval Date :
Application Number : 2456206
Regulatory Info : Ethical
Registration Country : Canada
Regulatory Info : Ethical
Registration Country : Canada
Brand Name : SMOFKABIVEN EXTRA NITROGEN
Dosage Form : EMULSION
Dosage Strength : 0.23G/100ML
Packaging :
Approval Date :
Application Number : 2501813
Regulatory Info : Ethical
Registration Country : Canada
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 :
Registration Country : Italy
isovaleric acid; Alpha-Glycerophosphoric Acid
Brand Name : Neurol
Dosage Form :
Dosage Strength : 10 Ampoules 2 Ml 41 Mg/2 Ml + 184 Mg/2 Ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Italy
Brand Name : Glicerovalerovit
Dosage Form :
Dosage Strength : 10 Vials 20 Mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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