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01 1AMINOLEVULINIC ACID HYDROCHLORIDE
02 1CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE)
03 1FLUOCINOLONE ACETONIDE
04 1GLYCOPYRROLATE
05 10METHOTREXATE
06 7METHOTREXATE (METHOTREXATE SODIUM)
07 1NAPROXEN
08 1POLYETHYLENE GLYCOL 3350
09 2RUPATADINE (RUPATADINE FUMARATE)
10 3TREOSULFAN
11 1Triamcinolone Hexacetonide
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01 12MEDEXUS
02 17Medexus Pharmaceuticals
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01 1POWDER
02 2POWDER FOR SOLUTION
03 2POWDER;INTRAVENOUS
04 11SOLUTION
05 10SOLUTION;SUBCUTANEOUS
06 1SUSPENSION
07 1Suspension for Injection
08 1TABLET
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01 10.025%/W/V
02 10.3%/W/V
03 11.5G/VIAL
04 1100%
05 110MG
06 110MG/0.20ML (10MG/0.20ML)
07 110MG/0.2ML
08 112.5MG/0.25ML
09 112.5MG/0.25ML (12.5MG/0.25ML)
10 115MG/0.30ML (15MG/0.30ML)
11 115MG/0.3ML
12 117.5MG/0.35ML
13 117.5MG/0.35ML (17.5MG/0.35ML)
14 11GM/VIAL
15 11MG/5ML
16 11MG/ML
17 120MG/0.4ML
18 120MG/0.4ML (20MG/0.4ML)
19 120MG/ML
20 122.5MG/0.45ML
21 122.5MG/0.45ML (22.5MG/0.45ML)
22 125MG/0.5ML
23 125MG/0.5ML (25MG/0.5ML)
24 125MG/ML
25 127.5MG/0.55ML (27.5MG/0.55ML)
26 130MG/0.6ML (30MG/0.6ML)
27 15G/VIAL
28 15GM/VIAL
29 17.5MG/0.15ML (7.5MG/0.15ML)
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01 17Canada
02 12USA
Regulatory Info : Prescription
Registration Country : Canada
AMINOLEVULINIC ACID HYDROCHLORIDE
Dosage Form : POWDER FOR SOLUTION
Brand Name : GLEOLAN
Dosage Strength : 1.5G/VIAL
Packaging :
Approval Date :
Application Number : 2504928
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE)
Dosage Form : SOLUTION
Brand Name : OTIXAL
Dosage Strength : 0.3%/W/V
Packaging : 0.25ML
Approval Date :
Application Number : 2459655
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : OTIXAL
Dosage Strength : 0.025%/W/V
Packaging : 0.25ML
Approval Date :
Application Number : 2459655
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : CUVPOSA
Dosage Strength : 1MG/5ML
Packaging :
Approval Date :
Application Number : 2469332
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;SUBCUTANEOUS
Brand Name : RASUVO
Dosage Strength : 10MG/0.20ML (10MG/0.20...
Packaging :
Approval Date : 2014-07-10
Application Number : 205776
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;SUBCUTANEOUS
Brand Name : RASUVO
Dosage Strength : 15MG/0.30ML (15MG/0.30...
Packaging :
Approval Date : 2014-07-10
Application Number : 205776
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;SUBCUTANEOUS
Brand Name : RASUVO
Dosage Strength : 17.5MG/0.35ML (17.5MG/...
Packaging :
Approval Date : 2014-07-10
Application Number : 205776
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;SUBCUTANEOUS
Brand Name : RASUVO
Dosage Strength : 22.5MG/0.45ML (22.5MG/...
Packaging :
Approval Date : 2014-07-10
Application Number : 205776
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;SUBCUTANEOUS
Brand Name : RASUVO
Dosage Strength : 27.5MG/0.55ML (27.5MG/...
Packaging :
Approval Date : 2014-07-10
Application Number : 205776
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;SUBCUTANEOUS
Brand Name : RASUVO
Dosage Strength : 30MG/0.6ML (30MG/0.6ML...
Packaging :
Approval Date : 2014-07-10
Application Number : 205776
Regulatory Info : RX
Registration Country : USA