01 3ADENOSINE
02 4AMCINONIDE
03 2AMPHOTERICIN B
04 1AVACINCAPTAD PEGOL SODIUM
05 1Amoxicillin
06 1Auranofin
07 5Bendamustine
08 1Bismuth Subcitrate
09 10CEFTIZOXIME SODIUM
10 2Capsaicin
11 3Cefixime
12 1Clavulanic acid
13 2ENFORTUMAB VEDOTIN-EJFV
14 4ENZALUTAMIDE
15 3ERLOTINIB HYDROCHLORIDE
16 3Enfortumab vedotin
17 1Enfortumab; Hypromellose
18 6Enzalutamide
19 1Enzalutamidum
20 1Erythromycin; Zinc Acetate
21 1FEZOLINETANT
22 1Fezolinetant
23 1GILTERITINIB FUMARATE
24 2Gilteritinib
25 1Gilteritinib Fumarate
26 1Gilteritinibum
27 8HYDROCORTISONE BUTYRATE
28 5Hydrocortisone
29 3ISAVUCONAZONIUM SULFATE
30 2Josamycin
31 9Leuprolide Acetate
32 2Lipiarmycin
33 5MICAFUNGIN SODIUM
34 2MIRABEGRON
35 4Micafungin
36 2Micafungin Sodium
37 2Micafunginum
38 13Mirabegron
39 4Mirabegronum
40 1Podophyllotoxin
41 1Potassium Chloride
42 1REGADENOSON
43 5Roxadustat
44 5SOLIFENACIN SUCCINATE
45 2Several substances refer to content
46 8Solifenacin
47 2Solifenacin Succinate
48 4Solifenacinum succinas
49 17TACROLIMUS
50 5TRIAMCINOLONE
51 16TRIAMCINOLONE ACETONIDE
52 1TRIAMCINOLONE DIACETATE
53 69Tacrolimus
54 9Tacrolimusum
55 3Tamsulosin
56 5Tamsulosin Hydrochloride
57 2Tamsulosin Hydrochloride; Solifenacin
58 3Tamsulosini hydrochloridum
59 1ZOLBETUXIMAB-CLZB
60 1Zinc Acetate
61 1aluminum phosphate
62 2barnidipine
63 1bendamustinhydroklorid
64 1capsaicin
65 1enzalutamid
66 1fidaxomicin
67 1hydrokortison
68 1interferon alfakon-1
69 2mikafunginnatrium
70 3solifenacinsuccinat
71 1tacrolimus (anhydrous)
72 7tacrolimus monohydrate
73 2takrolimus (vattenfri)
74 2takrolimusmonohydrat
01 67ASTELLAS
02 16ASTELLAS PHARMA CANADA INC
03 10ASTELLAS PHARMA EUROPE B.V.
04 4ASTELLAS PHARMA EUROPE BV
05 3ASTELLAS PHARMA GmbH
06 4ASTELLAS PHARMA SPA
07 27ASTELLAS PHARMA SpA
08 13Astellas
09 3Astellas Pharma
10 7Astellas Pharma (NUF)
11 27Astellas Pharma (Pty) Ltd
12 2Astellas Pharma - Kastrup
13 14Astellas Pharma A / S,
14 1Astellas Pharma A/S,
15 24Astellas Pharma AG
16 38Astellas Pharma Australia Pty Ltd
17 27Astellas Pharma Europe BV
18 13Astellas Pharma Europe BV,
19 2Astellas Pharma GmbH
20 1Astellas Pharma GmbH,
21 1FUJISAWA HLTHCARE
22 3OSI PHARMS
23 3YAMANOUCHI
01 7Antic-calc Tablet, Film Coated
02 2Antic-calc tablet Modified Release
03 1Auranofina 3Mg 30 Joined' Oral Use
04 1Barnidipina 10Mg 28 Combined Oral Use Rm
05 1Barnidipina 20Mg 28 Combined Oral Use Rm
06 1Bendamustina 100Mg 5 Units Parenteral Use
07 1Bendamustina 25Mg 20 Joined The Parenteral Use
08 1Bendamustina 25Mg 5 Units Parenteral Use
09 11CAP
10 4CAPSULE
11 4CAPSULE (EXTENDED RELEASE)
12 3CAPSULE, EXTENDED RELEASE;ORAL
13 6CAPSULE;ORAL
14 1CONCENTRATE FOR SOLUTION FOR INFUSION
15 3CREAM
16 12CREAM;TOPICAL
17 1CUTANEOUS EMULSION
18 1CUTANEOUS PATCH
19 1CUTANEOUS SOLUTION
20 1Capsaicin 179Mg 1 Patch Cutaneous Use
21 3Capsule, hard
22 1Capsule, soft
23 1Cefixima 2% 100Ml Oral Use
24 2Cefixima 400Mg 5 Units' Oral Use
25 1Concentrate to the infusion fluid
26 1Controlled Release Capsule
27 4Depot tablet
28 7Depottablett
29 2Dry Sub
30 1Enzalutamide 40Mg 112 Unita' Oral Use
31 1FILM COATED PILL
32 2FILMDRAGERAD TABLETT
33 2FOR SUSPENSION;ORAL
34 1Fidaxomicina 200Mg 20 Joined' Oral Use
35 1Filmtab
36 5Filmtabl
37 1GEL;TOPICAL
38 2GRANULAT TILL ORAL SUSPENSION
39 2Gran
40 2Granules to potion, suspension
41 3HARD CAPSULES
42 3Hard Capsules
43 1Hard Capsules With Extended Release-Oral
44 1Hard Release Capsules
45 2Hard Release Capsules - Oral
46 1Hudplaster
47 2Hydrocortisone 0.1% 30G Cream Dermatological Use
48 1Hydrocortisone 0.1% 30G Ointment Dermatological Use
49 1Hydrocortisone 0.1% 30Ml Solution Dermatological Use
50 2INJ
51 1INJECTABLE, LIPOSOMAL;INJECTION
52 1INJECTABLE; INJECTION
53 15INJECTABLE;INJECTION
54 2INJECTABLE;INTRAVENOUS
55 1Josamycin 1.000Mg 12 Combined Oral Use
56 1Josamycin 500Mg 12 Combined Oral Use
57 1KRÄM
58 3Kaps
59 1LOTION;TOPICAL
60 1Leuprorelin 22.5Mg 1 Unit Parenteral Use
61 1Leuprorelin 45Mg 1 Unit Parenteral Use
62 1Leuprorelin 7,5Mg 1 Unit Parenteral Use
63 1MODIFIED-RELEASE TABLET
64 1Micafungin 100Mg 10Ml 1 Units Parenteral Use
65 1Micafungin 50Mg 10Ml 1 Units Parenteral Use
66 1OINTMENT
67 8OINTMENT;TOPICAL
68 1ORAL SUSPENSION
69 2POI
70 3POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
71 3POWDER FOR SOLUTION
72 1POWDER;INTRAVENOUS
73 4PROLONGED-RELEASE CAPSULE, HARD
74 2PROLONGED-RELEASE TABLET
75 2PULVER TILL INFUSIONSVÄTSKA, LÖSNING
76 1PULVER TILL KONCENTRAT TILL
77 8Pit capsule, hard
78 1Potassium Chloride 600Mg 40 Combined Oral Use Rp
79 3Powder and liquid to the injection fluid, resolution in the finished filled syringe
80 2Powder for infusion fluid, resolution
81 2Powder to concentrate to the infusion fluid, resolution
82 4Ret Caps
83 7Ret Tablet
84 2SALVA
85 1SOFT CAPSULE
86 1SOLUTION
87 1SOLUTION FOR INJECTION
88 3SOLUTION;INTRAVENOUS
89 1SOLUTION;INTRAVITREAL
90 1SOLUTION;TOPICAL
91 1SUSPENSION;ORAL
92 1SYRUP;ORAL
93 12TAB
94 3TABLET
95 2TABLET (EXTENDED-RELEASE)
96 14TABLET;ORAL
97 1Tablet, film-coated
98 1Tacrolimus 0.5Mg 30 Joined' Oral Use
99 1Tacrolimus 0.5Mg 30 Joined' Oral Use Rp
100 1Tacrolimus 1Mg 60 Units Oral Use
101 1Tacrolimus 1Mg/Die 60 Units Oral Use Rp
102 1Tacrolimus 3Mg 30 Joined' Oral Use Rp
103 1Tacrolimus 5Mg 10 Units Parenteral Use
104 1Tacrolimus 5Mg 30 Joined' Oral Use
105 1Tacrolimus 5Mg 30 Joined' Oral Use Rp
106 2Tamsulosina 0,4Mg 20 Joined' Oral Use
107 15capsule
108 32Blank
01 10,03 %
02 10,1 %
03 10,2 MG
04 30.025%
05 10.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 110.1%
07 20.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 50.10%
09 10.2 mg
10 10.2mg
11 20.4 mg
12 10.4MG/5ML (0.08MG/ML)
13 50.4mg
14 20.5 MG
15 50.5 mg
16 40.5%
17 20.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 20.5MG
19 50.5mg
20 31 MG
21 11 MG/ML
22 101 mg
23 11 skin patch 179 mg + 1 gel cleanser
24 11 syringe 22.5 mg + Kit
25 11 syringe 7,5 mg + Kit
26 11 syringe groun soluz injector 45 mg + Kit
27 11 vial EV 100 mg 10 ml
28 11 vial EV 50 mg 10 ml
29 11%
30 110 Cpr Riv 5 Mg
31 110 MG
32 110 VIALS EV 5 mg 1 ml
33 310 mg
34 1100 MG
35 1100 mg
36 1100MG
37 1100MG/VIAL
38 3100mg
39 210MG
40 310mg
41 1112 cps Soft 40 MG
42 112 cpr dispers 1 g
43 112 cpr riv 500 mg
44 1120mg
45 1125mg
46 112mg
47 1150mg
48 116MG
49 1179 MG
50 1179 mg
51 1186MG
52 31MG
53 11MG/ML
54 61mg
55 12,5 MG/ML
56 22.5 mg/ml
57 120 VIALS EV 25 mg 2.5 mg/ml
58 220 cps 0.4 mg modified release
59 1200 MG
60 1200 MG / G + 45 MG / G
61 1200 mg
62 120MG/VIAL
63 120mg
64 122.5 MG
65 122.5 mg
66 125 MG
67 425 mg
68 125MG
69 325mg
70 126 Bust Gel Os 15 Ml 12.38 G
71 128 cps 10 mg modified release
72 128 cps 20 mg modified release
73 12MG
74 12MG/5ML
75 12x10 cpr riv 200 mg
76 13 MG
77 33 mg
78 130 Cpr Riv 5 Mg
79 130 cpr riv 3 mg
80 130 cps 0.5 mg
81 130 cps 0.5 mg prolonged release
82 130 cps 3 mg prolonged release
83 130 cps 5 mg
84 130 cps 5 mg prolonged release
85 130MG/VIAL
86 1372MG
87 13MG
88 13MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
89 13mg
90 140 CPR 600 mg prolonged release
91 140 MG
92 440 mg
93 440MG
94 340mg
95 145 MG
96 245 mg
97 145MG
98 14MG
99 35 MG
100 15 MG / ML
101 15 VIALS EV 100 mg 2,5 mg/ml
102 15 VIALS EV 25 mg 2.5 mg/ml
103 15 cpr orodispers 400 mg
104 15 cpr riv 400 mg
105 125 mg
106 15 mg/ml
107 250 MG
108 650 mg
109 4500 microgram
110 250MG
111 350MG/VIAL
112 650mg
113 45MG
114 15MG/ML
115 85mg
116 15mg/ml
117 16 MG / 0.4 MG
118 160 cps 1 mg
119 160 cps 1 mg prolonged release
120 160MG/20ML (3MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
121 26MG; 0.4MG
122 17.5 MG
123 17.5 mg
124 170mg
125 174.5MG
126 180MG
127 1875mg
128 18MG
129 19 MICROGRAMS
130 190MG/30ML (3MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
131 1EQ 0.2MG BASE/PACKET
132 2EQ 0.5MG BASE
133 1EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
134 1EQ 100MG BASE/VIAL
135 1EQ 10GM BASE/VIAL
136 1EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
137 2EQ 1GM BASE/VIAL
138 2EQ 1MG BASE
139 1EQ 1MG BASE/PACKET
140 2EQ 20MG BASE/ML
141 1EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
142 2EQ 2GM BASE/VIAL
143 1EQ 2MG BASE/0.1ML (EQ 2MG BASE/0.1ML)
144 1EQ 40MG BASE
145 2EQ 40MG BASE/ML
146 1EQ 500MG BASE/VIAL
147 1EQ 50MG BASE/VIAL
148 2EQ 5MG BASE
149 1EQ 5MG BASE/ML
150 1Emuls Derm 30 Ml
151 1Skin Soluz 3.5 Ml 0.5%
152 1Skin Soluz 4 % + 1,2 % + 1 Bottle Solv 30 Ml
153 1Ung Derm 10 G 0,1%
154 1Ung Derm 10 G 0.03%
155 1cream derm 30 g 0,1%
156 1cream hydrophilic derm 30 g 0,1%
157 1os grat suspe 100 ml 100 mg/5 ml
158 1soluz derm 30 ml 0.1%
159 1ung derm 30 g 0,1 g/100 g
160 24Blank
01 39Australia
02 17Canada
03 50Italy
04 44Norway
05 27South Africa
06 35Sweden
07 24Switzerland
08 74USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : ADENOCARD
Dosage Strength : 3MG/ML **Federal Regis...
Packaging :
Approval Date : 1989-10-30
Application Number : 19937
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : ADENOSCAN
Dosage Strength : 60MG/20ML (3MG/ML) **F...
Packaging :
Approval Date : 1995-05-18
Application Number : 20059
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : ADENOSCAN
Dosage Strength : 90MG/30ML (3MG/ML) **F...
Packaging :
Approval Date : 1995-05-18
Application Number : 20059
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Dosage Form :
Brand Name : Fosfalugel
Dosage Strength : 26 Bust Gel Os 15 Ml 1...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : CYCLOCORT
Dosage Strength : 0.025% **Federal Regis...
Packaging :
Approval Date : 1982-01-01
Application Number : 18116
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : CYCLOCORT
Dosage Strength : 0.1% **Federal Registe...
Packaging :
Approval Date : 1982-01-01
Application Number : 18116
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : OINTMENT;TOPICAL
Brand Name : CYCLOCORT
Dosage Strength : 0.1% **Federal Registe...
Packaging :
Approval Date : 1982-01-01
Application Number : 18498
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : LOTION;TOPICAL
Brand Name : CYCLOCORT
Dosage Strength : 0.1%
Packaging :
Approval Date : 1988-06-13
Application Number : 19729
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Africa
Dosage Form : TAB
Brand Name : Forcid Solutab 875/125
Dosage Strength : 875mg
Packaging : 10X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Brand Name : AMBISOME
Dosage Strength : 50MG/VIAL
Packaging : 1/10 VIALS (20 OR 30 ML VIALS)
Approval Date :
Application Number : 2241630
Regulatory Info : Prescription
Registration Country : Canada
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