01 10 Oxycodone Hydrochloride; Naloxone Hydrochloride Anhydrous
02 1Anhydroustheophylline
03 1Atropine Sulfate Monohydrate; Hydromorphone Hydrochloride
04 7Buprenorfin
05 26Buprenorphine
06 5Dorzolamide
07 3Dorzolamide + timolol
08 27Fluticasone Propionate; Formoterol Fumarate Dihydrate
09 6Fluticasone Propionate; Formoterol Fumarate Dihydric
10 3Flutikasonpropionat, Formoterolfumaratdihydrat
11 3Formoterol; Fluticasone
12 7Formoterol; Fluticasone Furoate
13 19Hydromorphone
14 42Hydromorphone Hydrochloride
15 1Ibuprofen; Codeine Phosphate Hemihydrate
16 5Leuprorelin
17 3Lidocaine Hydrochloride Monohydrate; Amylmetacresol; 2,4-Dichlorobenzyl Alcohol
18 1Lidocaine; Amylmetacresol; 2,4-Dichlorobenzylic Alcohol
19 2Malathion
20 12Morfinhemisulfat-2,5-Hydrat
21 42Morphine
22 11Morphine Sulfate
23 2Morphine Sulfate Pentahydrate
24 4Morphine Sulphate
25 19Morphine hemisulphate 2,5-hydrate
26 4Morphine sulfate
27 3Naloxone
28 4Naloxone Hydrochloride
29 2Naloxone Hydrochloride Dihydrate
30 16Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride
31 6Naloxone Hydrochloride; Oxycodone Hydrochloride
32 77Oxycodone
33 5Oxycodone (oxycodone) hydrochloride
34 4Oxycodone (oxycodone) hydrochloride/naloxone hydrochloride dihydrate
35 18Oxycodone + naloxone
36 63Oxycodone Hydrochloride
37 4Oxycodone; Naloxone
38 3Pegfilgrastim
39 2Povidone-Iodine
40 4Pralatrexate
41 15Prednisone
42 1REZAFUNGIN ACETATE
43 2Rezafungin Acetate
44 1Sennosides A & B
45 1Tafluprost
46 1Theophylline Anhydrous
47 9Timolol
48 14Tramadol Hydrochloride
49 11Tramadol hydrochloride
50 3Tramadolhydroklorid
51 1Zinc Sulfate Heptahydrate; Zinc Oxide
52 6fluticasone propionate + formoterol
53 3leuprorelin (&) bicalutamide
01 1MUNDIPHARMA
02 13MUNDIPHARMA PHARMACEUTIC. LLC
03 23MUNDIPHARMA PHARMACEUTIC.Srl
04 42Mundipharma (Pty) Ltd
05 115Mundipharma AS
06 94Mundipharma Ab
07 2Mundipharma Corporation (Ireland) Limited
08 2Mundipharma Gmbh
09 57Mundipharma Medical Company, Hamilton, Bermuda, Basel Branch
10 2Mundipharma Pharmaceuticals (Ireland) Limited
11 1Mundipharma Pharmaceuticals Limited
12 42Mundipharma Pharmaceuticals Sl
13 132Mundipharma Pty Limited
14 19Mundipharma Regulatory Gmbh
01 6Antic-calc tablet Modified Release
02 3CAP
03 27Capsule
04 8Capsule, hard
05 1Cutaneous Solution
06 2DOU
07 74Depot tablet
08 1EED
09 1Extended Release Capsule
10 1Extended Release Tablet
11 12Extended Release Tablets
12 4Extended-Release Hard Capsule
13 23Extended-Release Tablet
14 3Eye Drop
15 4Film 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 6Inhalation Solution
22 19Inhalation Spray
23 2Inhalation Suspension, Pressurized Container
24 3Inhalation aerosol, suspension
25 3Inhalational Suspension
26 3Injectable Solution
27 1Injectable Solution In Pre-Filled Syringe
28 2Injection
29 8Injection/infusion fluid, resolution
30 1LIQ
31 3Lozenge
32 1Melange
33 4Modified Release Capsule
34 34Modified Release Tablet
35 1Morphine Sulfate 100Mg 16 Combined Oral Use Rp
36 1Morphine Sulfate 10Mg 16 Combined Oral Use Rp
37 1Morphine Sulfate 30Mg 16 Combined Oral Use Rp
38 1Morphine Sulfate 60Mg 16 Combined Oral Use Rp
39 1Nasal Spray Solution
40 1Nasal Spray Solution In Single-Dose Container
41 7OPD
42 4Oral Solution
43 1Oral Spray
44 1Oxicodone 10Mg 28 Combined Oral Use Rp
45 1Oxicodone 20Mg 28 Combined Oral Use Rp
46 1Oxicodone 40Mg 28 Combined Oral Use Rp
47 1Oxicodone 5Mg 28 Combined Oral Use Rp
48 1Oxicodone 80Mg 28 Combined Oral Use Rp
49 1Oxicodone+Naloxone 10+5Mg 28 Combined Oral Use Rp
50 1Oxicodone+Naloxone 20+10Mg 28 Combined Oral Use Rp
51 1Oxicodone+Naloxone 40+20Mg 28 Combined Oral Use Rp
52 1Oxicodone+Naloxone+2,55 Mg 28 Combined Oral Use Rp
53 1POWDER;INTRAVENOUS
54 5PTD
55 1Paste
56 4Pit capsule, hard
57 1Potion, resolution
58 1Powder For Concentrate For Infusion Solution
59 1Powder For Concentrate For Solution For Infusion
60 1Prednisone 1Mg 30 Joined' Oral Use Rm
61 1Prednisone 2Mg 30 Joined' Oral Use Rm
62 1Prednisone 5Mg 30 Joined' Oral Use Rm
63 4Pressurised Inhalation Suspension
64 2Pressurized Inhalation Suspension
65 21SRT
66 1Solution
67 6Solution For Injection
68 12Solution For Injection/Infusion
69 7Suspension For Inhalation In Pressurized Container
70 3Sustained Release Capsule
71 56Tablet
72 7Transdermal Patch
73 7Transdermal patches
74 7capsule
75 7eye drops
76 4injection
77 15tablet
78 70Blank
01 40.5%
02 10.50%
03 21 mg
04 11 mg/ml
05 11%
06 11.3 mg
07 21.3mg
08 11.8MG
09 11.8mg
10 110 mcg/Hour
11 1510 mg
12 410 mg/5 mg
13 210 mg/mL
14 510 mg/ml
15 210 microgram/hour
16 7100 mg
17 1100MG
18 4100mg
19 710MG
20 110MG; 5 MG
21 210g/100ml
22 110mcg/hour
23 1610mg
24 210mg
25 810mg/ml
26 410mg;5mg
27 3120 doses suspe inhal 125 mcg + 5 mcg
28 2120 doses suspe inhal 250 mcg + 10 mcg
29 2120 doses suspe inhal 50 mcg + 5 mcg
30 1120 mg
31 3120mg
32 1125 microg/5 microg
33 2125MCG
34 3125MCG; 5 MCG
35 2125MCG; 5MCG
36 8125mcg/dose;5mcg/dose
37 1125mcg;5mcg
38 112mg
39 1142mg/71 ml
40 115 mcg/Hour
41 215 mg
42 215 mg/7.5 mg
43 6150 mg
44 1150MG
45 3150mg
46 315MG
47 115mcg/ml
48 115mcg/timme
49 115mg
50 215mg;7.5mg
51 116 CPR 10 mg prolonged release
52 116 CPR 100 mg prolonged release
53 116 CPR 30 mg prolonged release
54 116 CPR 60 mg prolonged release
55 116 mg
56 1160mg
57 116MG
58 316mg
59 11mg
60 11mg/ml
61 72 mg
62 22 mg/mL
63 12 mg/ml
64 32%
65 12.2mg/spray
66 12.5 mg/1.25 mg
67 22.5MG
68 12.5mg
69 22.5mg/ml
70 22.5mg;1.25mg
71 12.6 mg
72 22.6mg
73 120 mcg/Hour
74 720 mg
75 420 mg/10 mg
76 120 mg/ml
77 220 microgram/hour
78 7200 mg
79 3200MG
80 7200mg
81 1200mg/20ml
82 1200mg;30mg
83 520MG
84 320MG/1ML
85 120MG; 10 MG
86 120mcg/timme
87 1120mg
88 220mg
89 220mg/2ml
90 520mg/ml
91 420mg;10mg
92 122.5MG
93 124 mg
94 124MG
95 324mg
96 125 mcg/Hour
97 1250 microg/10 microg
98 2250MCG
99 2250MCG; 10MCG
100 5250mcg/dose;10mcg/dose
101 1250mcg;10mcg
102 125mcg/timme
103 128 CPR 10 mg prolonged release
104 128 CPR 20 mg prolonged release
105 128 CPR 40 mg + 20 mg prolonged release
106 128 CPR 40 mg prolonged release
107 128 CPR 5 mg prolonged release
108 128 CPR 80 mg prolonged release
109 128 cpr riv 10 mg + 5 mg prolonged release
110 128 cpr riv 20 mg + 10 mg prolonged release
111 128 cpr riv 5 mg + 2.5 mg prolonged release
112 22mg
113 32mg/ml
114 130 CPR 1 mg modified release
115 130 CPR 2 mg modified release bottle
116 130 CPR 5 mg modified release bottle
117 130 mcg/Hour
118 730 mg
119 230 mg/15 mg
120 2300 mg
121 1300MG
122 330MG
123 130mcg/timme
124 730mg
125 230mg;15mg
126 132mg
127 64 mg
128 140 mcg/Hour
129 440 mg
130 440 mg/20 mg
131 1400MG
132 1400mg
133 340MG
134 140MG; 20 MG
135 140mcg/timme
136 440mg
137 140mg
138 440mg;20mg
139 14MG
140 24mg
141 15 mcg/Hour
142 105 mg
143 45 mg/2.5 mg
144 25 microgram/hour
145 250 mg/ml
146 150 microg/5 microg
147 250MCG
148 350MCG; 5 MCG
149 250MCG; 5MCG
150 850mcg/dose;5mcg/dose
151 150mcg;5mcg
152 550mg/ml
153 55MG
154 15MG; 2.5 MG
155 135mg
156 25mg
157 35mg/ml
158 45mg;2.5mg
159 760 mg
160 1600mg
161 360MG
162 160MG; 30 MG
163 760mg
164 260mg;30mg
165 16MG
166 17.5MG
167 275 mg
168 175MG
169 68 mg
170 380 mg
171 380MG
172 180MG; 40 MG
173 580mg
174 280mg;40mg
175 18MG
176 28mg
177 190mg
178 1EQ 200MG BASE/VIAL
179 74Blank
01 132Australia
02 36Italy
03 115Norway
04 42South Africa
05 45Spain
06 98Sweden
07 76Switzerland
08 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
Mundipharma is a supplier offers 1 products (APIs, Excipients or Intermediates).
Find a price of FACILITIES AND CONTROLS bulk offered by Mundipharma
