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01 1Aluminum Chloride/Hydroxide (9:8:19:23)
02 14Atomoxetine Hydrochloride
03 1Bamipine lactate
04 2Calcitriol
05 2Calcium
06 6Cinacalcet Hydrochloride
07 3Dexamfetamine
08 4Dexamfetamine sulfate
09 6Dexamphetamine Sulfate
10 13Epoetin Alfa
11 1Iron
12 9Melatonin
13 20Methylphenidate Hydrochloride
14 11Methylphenidate hydrochloride
15 8Methylphenidati Hydrochloridum
16 1Oxybutynin
17 1Oxybutynin Hydrochloride
18 1Sevelamer Coals
19 1Sodium Bicarbonate
20 3Vadadustate
21 3Vadadustatum
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01 1MEDICE Health Family
02 18Medice Arzneimittel P?tter GmbH & Co KG
03 40Medice Arzneimittel P?tter Gmbh & Co. Kg
04 23Medice Arzneimittel Puetter Gmbh & Co. Kg
05 29Salmon Pharma Gmbh
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01 7Capsule
02 7Capsule For Inhalation
03 29Film Coated Tablet
04 1Gastro-Resistant Capsule
05 1Gel
06 1Hard Capsule
07 1Intravesical Solution
08 7Kapsel med modifisert frisetting, hard
09 7Modified-Release Hard Capsule
10 14Solution For Injection
11 1Solution For Injection/Infusion
12 35Tablet
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01 10.25mcg
02 10.5mcg
03 10.5mg
04 410 mg
05 110.000IU/ml
06 11000IU/0.5ml
07 1100MG
08 1100mg
09 410MG
10 710mg
11 2150mg
12 118MG
13 118mg
14 11mg
15 11mg/10ml
16 11mg/ml
17 12 mg
18 320 mg
19 120.000IU/0.5ml
20 12000IU/ml
21 420MG
22 620mg
23 120mg/5ml
24 125MG
25 125mg
26 12mg
27 130 mg
28 130.000IU/0.75ml
29 13000IU/0.3ml
30 3300mg
31 230MG
32 330mg
33 13mg
34 140 mg
35 140.000IU/ml
36 14000IU/0.4ml
37 240MG
38 340mg
39 2450mg
40 14mg
41 55 mg
42 150 mg
43 15000IU/0.5ml
44 3500mg
45 150MG
46 150mg
47 35MG
48 75mg
49 160 mg
50 16000IU/0.6ml
51 360MG
52 360mg
53 17000IU/0.7ml
54 18000IU/0.8ml
55 1800mg
56 180MG
57 180mg
58 19000IU/0.9ml
59 190MG
60 190mg
61 1mg
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01 1Germany
02 18Norway
03 23Spain
04 40Sweden
05 29Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Aluminum Chloride/hydroxide (9:8:19:23)
Dosage Form : Hard Capsule
Brand Name : Phosphonorm
Dosage Strength : 300mg
Packaging :
Approval Date : 17/02/1984
Application Number : 45866
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Audalis
Dosage Strength : 10mg
Packaging :
Approval Date : 07/02/2019
Application Number : 20171117000017
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Audalis
Dosage Strength : 100mg
Packaging :
Approval Date : 07/02/2019
Application Number : 20171117000079
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Audalis
Dosage Strength : 18mg
Packaging :
Approval Date : 07/02/2019
Application Number : 20171117000024
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Audalis
Dosage Strength : 25mg
Packaging :
Approval Date : 07/02/2019
Application Number : 20171117000031
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Audalis
Dosage Strength : 40mg
Packaging :
Approval Date : 07/02/2019
Application Number : 20171117000048
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Audalis
Dosage Strength : 60mg
Packaging :
Approval Date : 07/02/2019
Application Number : 20171117000055
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Audalis
Dosage Strength : 80mg
Packaging :
Approval Date : 07/02/2019
Application Number : 20171117000062
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Film Coated Tablet
Brand Name : Audalis
Dosage Strength : 100MG
Packaging :
Approval Date : 2019-04-30
Application Number : 84096
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Film Coated Tablet
Brand Name : Audalis
Dosage Strength : 25MG
Packaging :
Approval Date : 2019-04-30
Application Number : 84098
Regulatory Info : Cancelled
Registration Country : Spain