01 5ACETAMINOPHEN; HYDROCODONE BITARTRATE
02 2ALBUTEROL SULFATE
03 4ALPRAZOLAM
04 6AMITRIPTYLINE HYDROCHLORIDE
05 3AMPHETAMINE RESIN COMPLEX; DEXTROAMPHETAMINE RESIN COMPLEX
06 1ASPIRIN; HYDROCODONE BITARTRATE
07 1Atenolol
08 2Atenolol; Chlorthalidone
09 2BACLOFEN
10 1BICALUTAMIDE
11 4BIMEKIZUMAB
12 1BIMEKIZUMAB-BKZX
13 14BRIVARACETAM
14 2Bimekizumabum
15 24Brivaracetam
16 3CARBIDOPA; LEVODOPA
17 3CERTOLIZUMAB PEGOL
18 1CHLORPHENIRAMINE MALEATE; PSEUDOEPHEDRINE HYDROCHLORIDE
19 1CHLORPHENIRAMINE POLISTIREX; HYDROCODONE POLISTIREX
20 1CHLORPHENIRAMINE POLISTIREX; PHENYLPROPANOLAMINE POLISTIREX
21 1CROMOLYN SODIUM
22 26Certolizumab pegol
23 2Certolizumabum pegolum
24 5Cetirizine
25 2Colistin
26 1Colistin sodium methanesulfonate
27 16Cyclopentylcytosine
28 2DEXAMETHASONE SODIUM PHOSPHATE
29 1DIETHYLPROPION HYDROCHLORIDE
30 1Dl-Beta-Hydroxybutyric Acid Sodium Salt
31 2FAMOTIDINE
32 1FENFLURAMINE HYDROCHLORIDE
33 1Fenfluramine
34 1Ferrous Sulfate Glycine
35 1Ferrum(II) ionizate
36 1GLUTETHIMIDE
37 3HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE
38 2Hydroksyzinhydroklorid
39 3Hydroxyzine HCl
40 1Hydroxyzine dihydrochloridum
41 1Isosorbide Dinitrate
42 3Isosorbide-5-Mononitrate
43 11LACOSAMIDE
44 27LEVETIRACETAM
45 47Lacosamide
46 11Lacosamidum
47 9Lakosamide
48 24Levetiracetam
49 10Levetiracetamum
50 3Levocetirizine
51 4Levocetirizine dihydrochloride
52 1MIDAZOLAM
53 2MOEXIPRIL HYDROCHLORIDE
54 1Moexipril
55 1Moexipril; Hydrochlorothiazide
56 6Nitroglycerin
57 2PHENTERMINE RESIN COMPLEX
58 1PREDNISONE
59 1PSEUDOEPHEDRINE POLISTIREX
60 3Piracetam
61 12ROTIGOTINE
62 1ROZANOLIXIZUMAB-NOLI
63 1Romosozumabum
64 8Rotigotine
65 11Rotigotinum
66 1Sodium oxybas
67 4THEOPHYLLINE
68 3ZILUCOPLAN (ZILUCOPLAN SODIUM)
69 3ZILUCOPLAN SODIUM
70 8bimekizumab
71 14brivaracetam
72 1certolizumab pegol
73 3dixyrazin
74 1ferroglycinsulfatkomplex
75 1iron (II) glycinsulfat
76 4isosorbidmononitrat
77 8lakosamid
78 6levetiracetam
79 14rotigotine
80 1sodium oxybate
01 1KUDCO IRELAND
02 5SCHWARZ PHARMA
03 86UCB Australia Proprietary Limited
04 30UCB CANADA INC
05 77UCB INC
06 8UCB MANUFACTURING IRELAND LTD
07 8UCB Manufacturing Ireland Limited
08 14UCB Manufacturing Ireland Ltd.
09 2UCB Nordic AS
10 3UCB PHARMA GMBH
11 12UCB PHARMA S.A.
12 11UCB PHARMA SA
13 3UCB PHARMA SPA
14 25UCB PHARMA SpA
15 6UCB Pharma GmbH
16 1UCB Pharma Ltd
17 1UCB Pharma Ltd.
18 1UCB Pharma S.A
19 1UCB Pharma S.A.
20 8UCB Pharma S.A.,
21 16UCB Pharma SA
22 14UCB Pharma SA,
23 7UCB Pharma Said
24 11UCB SA
25 3UCB SA Pharma Sector
26 19UCB SAID
27 52UCB-Pharma SA
28 2WHITBY
01 1AEROSOL, METERED;INHALATION
02 1AEROSOL;NASAL
03 19Antic-calc Tablet, Film Coated
04 1Atenolol 100Mg 50 Combined Oral Use
05 1Atenolol+Chlorthalidone 100+25Mg 28 Combined Oral Use
06 1Atenolol+Chlorthalidone+12,550 Mg 28 Combined Oral Use
07 10CAPSULE, EXTENDED RELEASE;ORAL
08 1CAPSULE;ORAL
09 1CONCENTRATE FOR SOLUTION FOR INFUSION
10 1Caps
11 1Cetirizine 1% 20Ml Oral Use
12 1Cetirizine 10Mg 20 Joined' Oral Use
13 1Concentrate for infusion solution, solution
14 1Concentrate to the infusion fluid, resolution
15 3DEPOTKAPSEL, HÅRD
16 9FILM COATED PILL
17 6FILM, EXTENDED RELEASE;TRANSDERMAL
18 5FILMDRAGERAD TABLETT
19 1Ferrous Sulfate Glycine 100Mg 50 Combined Oral Use
20 2Film Coated Tablets
21 2Film-Coated Tablet
22 17Film-Coated Tablets
23 4Filmcoated Tablets Oral
24 11Filmtabl
25 1GASTRO-RESISTANT CAPSULE, HARD
26 1INFUSIONSVÄTSKA, LÖSNING
27 1INJECTABLE; INJECTION
28 1INJECTABLE;INJECTION
29 1INJECTABLE;INTRAVENOUS
30 1INJECTABLE;SUBCUTANEOUS
31 1INJECTION / INFUSION
32 1INJEKTIONSVÄTSKA, LÖSNING
33 1Infusion fluid, resolution
34 4Inj L?s
35 1Inj Sol
36 1Injection/infusion fluid, resolution
37 1Isosorbide Dinitrate 10Mg 10Ml 10 Units Parenteral Use
38 1Isosorbide Mononitrate 20Mg 50 Combined Oral Use
39 1Isosorbide Mononitrate 40Mg 30 Joined' Oral Use
40 1Isosorbide Mononitrate 50Mg 30 Joined' Oral Use
41 3L?s
42 1Lacosamide 100Mg 14 Joined' Oral Use
43 1Lacosamide 100Mg 56 Combined Oral Use
44 1Lacosamide 150Mg 14 Joined' Oral Use
45 1Lacosamide 150Mg 56 Combined Oral Use
46 1Lacosamide 200Mg 56 Combined Oral Use
47 1Lacosamide 50Mg 14 Joined' Oral Use
48 1Lacosamide 50Mg 56 Combined Oral Use
49 1Levetiracetam 1.000Mg 30 Joined' Oral Use
50 1Levetiracetam 100Mg/Ml 150Ml Bb 1-5Months Oral Use
51 1Levetiracetam 100Mg/Ml 150Ml Bb 6-48Months Oral Use
52 1Levetiracetam 100Mg/Ml 300Ml Oral Use
53 1Levetiracetam 500Mg 60 Units Oral Use
54 1Levocetirizina 5Mg 20 Joined' Oral Use
55 1Levocetirizina 5Mg/Ml 20Ml Oral Use
56 11Matrixpfl
57 4Mixture, solution
58 1Moexipril 15Mg 14 Joined' Oral Use
59 1Moexipril+Hydrochlorothiazide 25+15Mg 14 Joined' Oral Use
60 2Nitroglycerin 10Mg/Die 15 Plasters Transdermal Use
61 2Nitroglycerin 15Mg/Die 15 Plasters Transdermal Use
62 2Nitroglycerin 5Mg/Die 15 Plasters Transdermal Use
63 1ORAL DROPS, SOLUTION
64 3ORAL SOLUTION
65 1Oral Drops, Solution
66 1Oral Solution
67 1Oral Solution - 300 Ml
68 1Oral Solution Bottle (Glass) 150
69 6PATCH
70 5Potion, resolution
71 1Rotigotina 2Mg/Day 7 Plasters Transdermal Use
72 1Rotigotina 2Mg/Die 28 Plasters Transdermal Use
73 1Rotigotina 4Mg/Day 7 Plasters Transdermal Use
74 1Rotigotina 4Mg/Die 28 Plasters Transdermal Use
75 1Rotigotina 6Mg/Day 7 Plasters Transdermal Use
76 1Rotigotina 6Mg/Die 28 Plasters Transdermal Use
77 1Rotigotina 8Mg/Day 7 Plasters Transdermal Use
78 1Rotigotina 8Mg/Die 28 Plasters Transdermal Use
79 2SIRAP
80 12SOLUTION
81 1SOLUTION FOR INJECTION, PRE-FILLED SYRINGE
82 2SOLUTION;INTRAVENOUS
83 4SOLUTION;ORAL
84 3SOLUTION;SUBCUTANEOUS
85 1SPRAY;NASAL
86 3SUSPENSION, EXTENDED RELEASE;ORAL
87 1Sirup
88 3Solution
89 1Solution for infusion
90 1Solution for injection/infusion
91 2Syrup
92 12TABLET
93 2TABLET, EXTENDED RELEASE;ORAL
94 11TABLET, ORALLY DISINTEGRATING;ORAL
95 36TABLET;ORAL
96 3TABLETT
97 14TRANSDERMAL PATCH
98 1Tabl
99 21Tablet, film-coated
100 8Transdermal patches
101 1Tropfen
102 13injection
103 2oral
104 19tablet
105 61Blank
01 10.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 10.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 21 MG / 24 H
04 11 Vial 1,000,000 Iu 4 Ml + Vial Solv
05 21 g
06 210 MG
07 210 MG / ML
08 310 MG/ML
09 110 VIALS EV 10 mg 10 ml
10 410 mg
11 910 mg/ml
12 4100 MG
13 2100 MG / ML
14 10100 mg
15 2100 mg/mL
16 11100 mg/ml
17 11000 MG
18 71000 mg
19 31000mg
20 6100MG
21 1100MG/ML
22 5100mg
23 3100mg/ml
24 1105mg/1.17ml
25 310MG
26 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 510MG/ML
28 110MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
29 110mg
30 310mg/ml
31 112 Vials Os Ev 3 G 15 Ml
32 112.5MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
33 112.5MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
34 112MG;120MG
35 2130MG
36 114 cpr riv 100 mg
37 114 cpr riv 15 mg
38 114 cpr riv 15 mg + 25 mg
39 114 cpr riv 150 mg
40 114 cpr riv 50 mg
41 115 MG/ML
42 215 plasters transd 10 mg/day
43 215 plasters transd 15 mg/day
44 215 transd plasters 5 mg/day
45 1150 MG
46 7150 mg
47 3150MG
48 3150mg
49 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
50 116.6MG/0.416ML
51 2160MG/ML
52 1160ML
53 2160mg/ml
54 11GM
55 11MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
56 11MG/24HOUR
57 11MG/24HR
58 21mg/24h
59 22 MG / 24 H
60 42 mg/24 hours
61 120 Cpr Riv Div 25 Mg
62 120 MG
63 120 cpr riv 10 mg
64 120 cpr riv 5 mg
65 2200 MG
66 7200 mg
67 13200 mg/mL
68 3200MG
69 1200MG/20ML (10MG/ML)
70 2200MG/ML
71 3200mg
72 2200mg/ml
73 120MG
74 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
75 123MG/0.574ML
76 325 MG
77 325 mg
78 1250 MG
79 6250 mg
80 2250MG
81 1250mg
82 425MG
83 125MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
84 125MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
85 125MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
86 225mg
87 2260MG
88 128 CPR 100 mg + 25 mg
89 128 CPR 50 mg + 12.5mg
90 128 transd plasters 2 mg/day
91 128 transd plasters 4 mg/day
92 128 transd plasters 6 mg/day
93 128 transd plasters 8 mg/day
94 1280MG/2ML(140MG/ML)
95 12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
96 12MG/24HOUR
97 12MG/24HR
98 22mg/24h
99 23 MG / 24 H
100 130 MG / ML
101 130 cpr div 40 mg
102 130 cpr riv 1,000 mg
103 130 cps 50 mg prolonged release
104 132.4MG/0.81ML
105 2320MG/2ML
106 13MG/24HOUR
107 13MG/24HR
108 23mg/24h
109 24 MG / 24 H
110 44 mg/24 hours
111 140 Cpr Riv 1.200 Mg
112 140MG
113 14MG/24HOUR
114 14MG/24HR
115 24mg/24h
116 15 mg
117 150 CPR 100 mg
118 350 MG
119 150 MG + 100 MG
120 150 cpr div 20 mg
121 150 cps gastrores 100 mg
122 1350 mg
123 1500 MG
124 1500 MG / ML
125 7500 mg
126 1500 mg/ml
127 4500MG
128 1500MG/5ML (100MG/ML)
129 2500MG;10MG
130 2500MG;5MG
131 1500MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
132 3500mg
133 1500mg/ml
134 650MG
135 150MG/5ML (10MG/ML)
136 250mg
137 156 cpr riv 100 mg
138 156 cpr riv 150 mg
139 156 cpr riv 200 mg
140 156 cpr riv 50 mg
141 15MG
142 15MG/SPRAY
143 35mg
144 16 Ampoules Im Ev 100 Mg 2 Ml
145 26 MG / 24 H
146 46 mg/24 hours
147 160 cpr riv 500 mg
148 1650MG;7.5MG
149 16MG/24HOUR
150 16MG/24HR
151 26mg/24h
152 17 transd plasters 2 mg/day
153 17 transd plasters 4 mg/day
154 17 transd plasters 6 mg/day
155 17 transd plasters 8 mg/day
156 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
157 175 MG
158 275 mg
159 1750 MG
160 3750MG
161 375MG
162 175mg
163 18 Cpr 1,500,000 Iu
164 28 MG / 24 HOURS
165 28 mg/24 hours
166 1800mg
167 18MG/24HOUR
168 18MG/24HR
169 18mg/24h
170 1Bb Scir 150 Ml 0.1%
171 2EQ 0.1MG PHOSPHATE/INH
172 1EQ 10MG BASE;EQ 10MG BASE
173 1EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
174 1EQ 16.6MG BASE/0.416ML (EQ 16.6MG BASE/0.416ML)
175 1EQ 2.2MG BASE/ML
176 1EQ 23MG BASE/0.574ML (EQ 23MG BASE/0.574ML)
177 1EQ 2MG BASE
178 1EQ 3.75MG BASE;EQ 3.75MG BASE
179 1EQ 30MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
180 1EQ 32.4MG BASE/0.81ML (EQ 32.4 BASE/0.81ML)
181 1EQ 4MG BASE
182 1EQ 4MG MALEATE/5ML;EQ 37.5MG HCL/5ML
183 1EQ 6.25MG BASE;EQ 6.25MG BASE
184 1EQ 60MG HYDROCHLORIDE/5ML
185 1EQ 8MG MALEATE/5ML;EQ 10MG BITARTRATE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
186 1Gtt Os 4,000,000 Iu 4 Ml
187 2POWER SERIES
188 1The Scir 150 Ml 0.2%
189 1os gtt 20 ml 10 mg/ml
190 1os gtt 20 ml 5 mg/ml
191 1os soluz 1 Bottle 300 ml 100 mg/ml + 1 syringe
192 1os soluz 150 ml 100 mg/ml + 1 syringe 1 ml
193 1os soluz 150 ml 100 mg/ml + 1 syringe 3 ml
194 47Blank
01 86Australia
02 30Canada
03 63Italy
04 65Norway
05 46Sweden
06 52Switzerland
07 85USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : LORTAB
Dosage Strength : 500MG;10MG
Packaging :
Approval Date : 1996-01-26
Application Number : 40100
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 650MG;7.5MG
Packaging :
Approval Date : 1996-11-21
Application Number : 40134
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 500MG;10MG
Packaging :
Approval Date : 1997-08-13
Application Number : 40210
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : LORTAB
Dosage Strength : 500MG;5MG
Packaging :
Approval Date : 1982-07-09
Application Number : 87722
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : CO-GESIC
Dosage Strength : 500MG;5MG
Packaging :
Approval Date : 1982-05-03
Application Number : 87757
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ALBUTEROL SULFATE
Dosage Strength : EQ 2MG BASE
Packaging :
Approval Date : 1992-09-29
Application Number : 73120
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ALBUTEROL SULFATE
Dosage Strength : EQ 4MG BASE
Packaging :
Approval Date : 1992-09-29
Application Number : 73121
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, ORALLY DISINTEGR...
Brand Name : NIRAVAM
Dosage Strength : 0.25MG **Federal Regis...
Packaging :
Approval Date : 2005-01-19
Application Number : 21726
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, ORALLY DISINTEGR...
Brand Name : NIRAVAM
Dosage Strength : 0.5MG **Federal Regist...
Packaging :
Approval Date : 2005-01-19
Application Number : 21726
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, ORALLY DISINTEGR...
Brand Name : NIRAVAM
Dosage Strength : 2MG **Federal Register...
Packaging :
Approval Date : 2005-01-19
Application Number : 21726
Regulatory Info : DISCN
Registration Country : USA
Ucb Pharma S.a is a supplier offers 14 products (APIs, Excipients or Intermediates).
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