01 10 Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
02 1Ambroxol Hydrochloride
03 1Anhydroustheophylline
04 1Atropine Sulfate Monohydrate; Hydromorphone Hydrochloride
05 7Buprenorfin
06 26Buprenorphine
07 1Choline Salicylate
08 5Dorzolamide
09 3Dorzolamide + timolol
10 27Fluticasone Propionate; Formoterol Fumarate Dihydrate
11 6Fluticasone Propionate; Formoterol Fumarate Dihydric
12 3Fluticasone Propionate; Formoterol fumarate dihydrate
13 7Formoterol; Fluticasone Furoate
14 19Hydromorphone
15 32Hydromorphone Hydrochloride
16 2Hydromorphone hydrochloride
17 1Ibuprofen; Codeine Phosphate Hemihydrate
18 5Leuprorelin
19 3Lidocaine Hydrochloride Monohydrate; Amylmetacresol; 2,4-Dichlorobenzyl Alcohol
20 1Lidocaine; Amylmetacresol; 2,4-Dichlorobenzylic Alcohol
21 2Malathion
22 12Morfinhemisulfat-2,5-Hydrat
23 45Morphine
24 11Morphine Sulfate
25 2Morphine Sulfate Pentahydrate
26 4Morphine Sulphate
27 13Morphine hemisulfate 2.5-hydrate
28 4Morphine sulfate
29 4Naloxone
30 4Naloxone Hydrochloride
31 2Naloxone Hydrochloride Dihydrate
32 16Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride
33 6Naloxone Hydrochloride; Oxycodone Hydrochloride
34 1Naloxone hydrochloride dihydrate
35 32Oxycodone
36 5Oxycodone (oxycodone) hydrochloride
37 4Oxycodone (oxycodone) hydrochloride/naloxone hydrochloride dihydrate
38 18Oxycodone + naloxone
39 63Oxycodone Hydrochloride
40 30Oxycodone hydrochloride
41 16Oxycodone hydrochloride; Naloxone hydrochloride dihydrate
42 8Oxycodone; Naloxone
43 1Oxycodone; Oxycodone Hydrochloride
44 5Pegfilgrastim
45 9Povidone-Iodine
46 4Pralatrexate
47 12Prednisone
48 1REZAFUNGIN ACETATE
49 2Rezafungin Acetate
50 1Rezafungin acetate
51 1Sennosides A & B
52 1Tafluprost
53 1Theophylline Anhydrous
54 11Timolol
55 5Tramadol Hydrochloride
56 2Tramadol hydrochloride
57 12Tramadolhydroklorid
58 1Zinc Sulfate Heptahydrate; Zinc Oxide
59 6fluticasone propionate + formoterol
60 3leuprorelin (&) bicalutamide
01 1MUNDIPHARMA
02 13MUNDIPHARMA PHARMACEUTIC. LLC
03 23MUNDIPHARMA PHARMACEUTIC.Srl
04 42Mundipharma (Pty) Ltd
05 80Mundipharma AS
06 94Mundipharma Ab
07 6Mundipharma Corporation (Ireland) Limited
08 3Mundipharma Corporation Limited
09 11Mundipharma Ges.M.B.H.
10 3Mundipharma Gmbh
11 57Mundipharma Medical Company, Hamilton, Bermuda, Basel Branch
12 2Mundipharma Pharmaceuticals (Ireland) Limited
13 10Mundipharma Pharmaceuticals Limited
14 43Mundipharma Pharmaceuticals Sl
15 134Mundipharma Pty Limited
16 19Mundipharma Regulatory Gmbh
01 3CAP
02 33Capsule
03 1Cutaneous Powder
04 5Cutaneous Solution
05 2DOU
06 1EED
07 1Ear Drop Suspension
08 1Extended Release Capsule
09 1Extended Release Tablet
10 12Extended Release Tablets
11 4Extended-Release Hard Capsule
12 23Extended-Release Tablet
13 3Eye Drop
14 4Film Coated Tablet
15 2Film-Coated Tablet
16 3Fluticasone+Formoterol 125+5Mcg 120 Unita' Respiratory Use
17 2Fluticasone+Formoterol 250+10Mcg 120 Unita' Respiratory Use
18 2Fluticasone+Formoterol 50+5Mcg 120 Unita' Respiratory Use
19 3Hard Capsule
20 2INJ
21 3Inhalation Aerosol
22 6Inhalation Solution
23 20Inhalation Spray
24 2Inhalation Suspension, Pressurized Container
25 1Injectable And Infusion Solution
26 3Injectable Solution
27 1Injectable Solution In Pre-Filled Syringe
28 2Injection
29 1LIQ
30 3Lozenge
31 4Modified Release Capsule
32 37Modified Release Tablet
33 1Morphine Sulfate 100Mg 16 Combined Oral Use Rp
34 1Morphine Sulfate 10Mg 16 Combined Oral Use Rp
35 1Morphine Sulfate 30Mg 16 Combined Oral Use Rp
36 1Morphine Sulfate 60Mg 16 Combined Oral Use Rp
37 1Nasal Spray Solution
38 2Nasal Spray Solution In Single-Dose Container
39 7OPD
40 4Oral Solution
41 1Oral Spray
42 1Oromucosal Solution
43 1Oxicodone 10Mg 28 Combined Oral Use Rp
44 1Oxicodone 20Mg 28 Combined Oral Use Rp
45 1Oxicodone 40Mg 28 Combined Oral Use Rp
46 1Oxicodone 5Mg 28 Combined Oral Use Rp
47 1Oxicodone 80Mg 28 Combined Oral Use Rp
48 1Oxicodone+Naloxone 10+5Mg 28 Combined Oral Use Rp
49 1Oxicodone+Naloxone 20+10Mg 28 Combined Oral Use Rp
50 1Oxicodone+Naloxone 40+20Mg 28 Combined Oral Use Rp
51 1Oxicodone+Naloxone+2,55 Mg 28 Combined Oral Use Rp
52 1POWDER;INTRAVENOUS
53 5PTD
54 1Paste
55 1Powder For Concentrate For Infusion Solution
56 2Powder For Concentrate For Solution For Infusion
57 1Prednisone 1Mg 30 Joined' Oral Use Rm
58 1Prednisone 2Mg 30 Joined' Oral Use Rm
59 1Prednisone 5Mg 30 Joined' Oral Use Rm
60 4Pressurised Inhalation Suspension
61 2Pressurized Inhalation Suspension
62 1Prolonged Release Capsule Hard
63 21SRT
64 1Solution
65 8Solution For Injection
66 18Solution For Injection/Infusion
67 7Suspension For Inhalation In Pressurized Container
68 3Sustained Release Capsule
69 3Syrup
70 120Tablet
71 14Transdermal Patch
72 1Vaginal Solution
73 7capsule
74 9eye drops
75 4injection
76 15tablet
77 70Blank
01 60.5%
02 10.50%
03 11%
04 11%W/V
05 21.3mg
06 11.8MG
07 21.8mg
08 610 mg
09 110 mg/5 mg
10 210 mg/mL
11 210 microgram/hour
12 410%W/V
13 1100 mg
14 1100MG
15 8100mg
16 810MG
17 110MG; 5 MG
18 210g/100ml
19 210mcg/hour
20 2410mg
21 210mg
22 1210mg/ml
23 410mg; 5mg
24 410mg;5mg
25 3120 doses suspe inhal 125 mcg + 5 mcg
26 2120 doses suspe inhal 250 mcg + 10 mcg
27 2120 doses suspe inhal 50 mcg + 5 mcg
28 4120mg
29 2125MCG
30 3125MCG; 5 MCG
31 1125MCG; 5MCG
32 8125mcg/dose;5mcg/dose
33 1125mcg; 5mcg
34 1125mcg;5mcg
35 112mg
36 1142mg/71 ml
37 1150MG
38 6150mg
39 315MG
40 115mcg/hour
41 115mcg/ml
42 115mcg/timme
43 215mg
44 215mg; 7.5mg
45 215mg;7.5mg
46 116 CPR 10 mg prolonged release
47 116 CPR 100 mg prolonged release
48 116 CPR 30 mg prolonged release
49 116 CPR 60 mg prolonged release
50 1160mg
51 116MG
52 316mg
53 118mg/0.1ml
54 11MG
55 11mg
56 21mg/ml
57 52 mg
58 22 mg/mL
59 32%
60 12.2mg/spray
61 12.5%W/W
62 22.5MG
63 12.5mg
64 22.5mg/ml
65 22.5mg;1.25mg
66 22.6mg
67 220 mg
68 120 mg/10 mg
69 220 microgram/hour
70 120%W/V
71 3200MG
72 12200mg
73 1200mg/20ml
74 1200mg;30mg
75 520MG
76 320MG/1ML
77 120MG; 10 MG
78 120mcg/hour
79 120mcg/timme
80 1820mg
81 220mg
82 220mg/2ml
83 520mg/ml
84 420mg; 10mg
85 420mg;10mg
86 122.5MG
87 124MG
88 324mg
89 2250MCG
90 1250MCG; 10MCG
91 5250mcg/dose;10mcg/dose
92 1250mcg; 10mcg
93 1250mcg;10mcg
94 125mcg/hour
95 125mcg/timme
96 128 CPR 10 mg prolonged release
97 128 CPR 20 mg prolonged release
98 128 CPR 40 mg + 20 mg prolonged release
99 128 CPR 40 mg prolonged release
100 128 CPR 5 mg prolonged release
101 128 CPR 80 mg prolonged release
102 128 cpr riv 10 mg + 5 mg prolonged release
103 128 cpr riv 20 mg + 10 mg prolonged release
104 128 cpr riv 5 mg + 2.5 mg prolonged release
105 12MG
106 22mg
107 42mg/ml
108 130 CPR 1 mg modified release
109 130 CPR 2 mg modified release bottle
110 130 CPR 5 mg modified release bottle
111 130 mg
112 1300MG
113 1300mg
114 330MG
115 130mcg/hour
116 130mcg/timme
117 1330mg
118 230mg; 15mg
119 230mg;15mg
120 132mg
121 54 mg
122 140 mg
123 140 mg/20 mg
124 1400MG
125 1400mg
126 340MG
127 140MG; 20 MG
128 140mcg/hour
129 140mcg/timme
130 840mg
131 140mg
132 440mg; 20mg
133 440mg;20mg
134 14MG
135 24mg
136 35 mg
137 15 mg/2.5 mg
138 25 microgram/hour
139 250MCG
140 350MCG; 5 MCG
141 150MCG; 5MCG
142 850mcg/dose;5mcg/dose
143 150mcg; 5mcg
144 150mcg;5mcg
145 750mg/ml
146 65MG
147 15MG; 2.5 MG
148 15ML
149 15mcg/hour
150 135mg
151 25mg
152 35mg/ml
153 35mg; 2.5mg
154 15mg; 25mg
155 45mg;2.5mg
156 160 mg
157 1600mg
158 360MG
159 160MG; 30 MG
160 1260mg
161 260mg;30mg
162 16MG
163 26mg/0.6ml
164 17.5%W/V
165 17.5MG
166 175MG
167 175mg
168 58 mg
169 380MG
170 180MG; 40 MG
171 980mg
172 280mg;40mg
173 18MG
174 28mg
175 190mg
176 1EQ 200MG BASE/VIAL
177 78Blank
01 134Australia
02 15Estonia
03 36Italy
04 12Malta
05 81Norway
06 42South Africa
07 46Spain
08 98Sweden
09 76Switzerland
10 1USA
Regulatory Info : Allowed
Registration Country : Switzerland
Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
Dosage Form : Modified Release Tablet
Brand Name : Targin mg
Dosage Strength : 10mg;5mg
Packaging :
Approval Date : 13/11/2009
Application Number : 58683
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
Dosage Form : Modified Release Tablet
Brand Name : Targin mg
Dosage Strength : 20mg;10mg
Packaging :
Approval Date : 13/11/2009
Application Number : 58683
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
Dosage Form : Modified Release Tablet
Brand Name : Targin
Dosage Strength : 5mg;2.5mg
Packaging :
Approval Date : 13/11/2009
Application Number : 58683
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
Dosage Form : Modified Release Tablet
Brand Name : Targin mg
Dosage Strength : 40mg;20mg
Packaging :
Approval Date : 13/11/2009
Application Number : 58683
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
Dosage Form : Modified Release Tablet
Brand Name : Targin mg
Dosage Strength : 60mg;30mg
Packaging :
Approval Date : 13/11/2009
Application Number : 58683
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
Dosage Form : Modified Release Tablet
Brand Name : Targin mg
Dosage Strength : 80mg;40mg
Packaging :
Approval Date : 13/11/2009
Application Number : 58683
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
Dosage Form : Modified Release Tablet
Brand Name : OxycodoneNaloxone Mundiph...
Dosage Strength : 10mg;5mg
Packaging :
Approval Date : 17/05/2023
Application Number : 69358
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
Dosage Form : Modified Release Tablet
Brand Name : OxycodoneNaloxone Mundiph...
Dosage Strength : 20mg;10mg
Packaging :
Approval Date : 17/05/2023
Application Number : 69358
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
Dosage Form : Modified Release Tablet
Brand Name : OxycodoneNaloxone Mundiph...
Dosage Strength : 5mg;2.5mg
Packaging :
Approval Date : 17/05/2023
Application Number : 69358
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
Dosage Form : Modified Release Tablet
Brand Name : OxycodoneNaloxone Mundiph...
Dosage Strength : 40mg;20mg
Packaging :
Approval Date : 17/05/2023
Application Number : 69358
Regulatory Info : Allowed
Registration Country : Switzerland
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