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01 3ADALIMUMAB
02 2ADALIMUMAB-ATTO
03 1AFLIBERCEPT-AYYH
04 7APREMILAST
05 1AVACOPAN
06 3Adalimumab
07 16Adalimumabum
08 3Apremilast
09 1Apremilastum
10 1April eve
11 2BEVACIZUMAB
12 2BEVACIZUMAB-AWWB
13 2BLINATUMOMAB
14 4Bevacizumab
15 2Bevacizumabum
16 11Blinatumomab
17 1Blinatumomabum
18 6CARFILZOMIB
19 3CINACALCET HYDROCHLORIDE
20 2CYSTEAMINE (CYSTEAMINE BITARTRATE)
21 4CYSTEAMINE BITARTRATE
22 22Carfilzomib
23 3Carfilzomibum
24 3Cinacalcet
25 6Cinacalcet Hydrochloride
26 3Cinacalcetum
27 24DARBEPOETIN ALFA
28 4DENOSUMAB
29 1DICLOFENAC SODIUM
30 36Darbepoetin alfa
31 11Darbepoetinum alfa
32 5Denosumab
33 2Denosumabum
34 1ECULIZUMAB-AEEB
35 7EPOETIN ALFA
36 1ERENUMAB-AOOE
37 2ESOMEPRAZOLE MAGNESIUM; NAPROXEN
38 3ETANERCEPT
39 3ETELCALCETIDE
40 4EVOLOCUMAB
41 3Etelcalcetide
42 4Evolocumab
43 2Evolocumabum
44 4Evolokumab
45 1FAMOTIDINE; IBUPROFEN
46 16FILGRASTIM
47 3Filgrastim
48 3Filgrastimum ADNr
49 2GLYCEROL PHENYLBUTYRATE
50 1INEBILIZUMAB
51 1INFLIXIMAB
52 1INFLIXIMAB-AXXQ
53 1INTERFERON GAMMA-1B
54 1IVABRADINE
55 2IVABRADINE HYDROCHLORIDE
56 1LEVOFLOXACIN (LEVOFLOXACIN HEMIHYDRATE)
57 1LEVOMEPROMAZINE
58 1OXALIPLATIN
59 2PAMIDRONATE DISODIUM
60 5PANITUMUMAB
61 2PEGFILGRASTIM
62 1PEGLOTICASE
63 3PREDNISONE
64 9Panitumumab
65 2Panitumumabum
66 1Pegfilgrastim
67 1Pegfilgrastimum
68 1RITUXIMAB-ARRX
69 3ROMIPLOSTIM
70 1ROMOSOZUMAB
71 1ROMOSOZUMAB-AQQG
72 8Romiplostim
73 2Romosozumab
74 2SODIUM PHENYLBUTYRATE
75 4SOTORASIB
76 4Su 5416
77 2TARLATAMAB
78 2TARLATAMAB-DLLE
79 1TEPROTUMUMAB-TRBW
80 2THIOTEPA
81 2TRASTUZUMAB
82 2TRASTUZUMAB-ANNS
83 2Talimogenum laherparepvecum
84 2Trastuzumabum
85 6USTEKINUMAB
86 3USTEKINUMAB-AUUB
87 1blinatumomab
88 2cinacalcet
89 3cinakalcethydroklorid
90 36darbepoetin alfa
91 3denosumab
92 2evolokumab
93 3filgrastim
94 1karfilzomib
95 1panitumumab
96 2pegfilgrastim
97 4romiplostim
98 2talimogen laherparepvek
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01 32AMGEN
02 51AMGEN CANADA INC
03 8AMGEN EUROPE B.V.
04 3AMGEN EUROPE BV
05 27AMGEN INC
06 85Amgen Australia Pty Limited
07 21Amgen Europe B.V.
08 52Amgen Europe BV
09 6Amgen Inc
10 21Amgen South Africa (Pty) Ltd
11 58Amgen Switzerland AG
12 1CHEMOCENTRYX
13 11HORIZON
14 1HORIZON PHARMA
15 3HORIZON THERAP US
16 1HORIZON THERAPEUTICS IRELAND
17 6HORIZON THERAPEUTICS IRELAND DAC
18 5IMMUNEX
19 1IMMUNEX CORPORATION
20 3KAI PHARMS INC
21 2MN PHARMS
22 1MUSTAFA NEVSAT IIAC SANAYII A.S.
23 3ONYX PHARMS AMGEN
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01 3Antic-calc Tablet, Film Coated
02 2CAPSULE (DELAYED RELEASE)
03 2CAPSULE, DELAYED RELEASE;ORAL
04 1CAPSULE;ORAL
05 1Cinacalcet 30Mg 28 Combined Oral Use
06 1Cinacalcet 60Mg 28 Combined Oral Use
07 1Cinacalcet 90Mg 28 Combined Oral Use
08 9Dry Sub
09 1FCT
10 3FILMDRAGERAD TABLETT
11 2Filgrastim 30,000.000Iu 1 Unit Parenteral Use
12 7Film-Coated Tablets
13 1Filmtabl
14 2GRANULE, DELAYED RELEASE;ORAL
15 17INJ
16 4INJECTABLE; INJECTION
17 3INJECTABLE; IV (INFUSION)
18 3INJECTABLE; SUBCUTANEOUS
19 18INJECTABLE;INJECTION
20 3INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
21 1INJEKTIONSVÄTSKA, LÖSNING I FÖRFYLLD
22 2INJEKTIONSVÄTSKA, LÖSNING, FÖRFYLLD SPRUTA
23 1Including
24 4Inf Conc
25 1Inj
26 25Inj L?s
27 3Inj Sol
28 1Inj Soluble
29 10Inj Solution
30 2Injection fluid, resolution
31 4Injection fluid, resolution/concentrate to the infusion fluid
32 1KIT
33 1KONCENTRAT TILL INFUSIONSVÄTSKA, LÖSNING
34 1LIQUID
35 1LIQUID;ORAL
36 1PFP
37 5PFS
38 2POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
39 1POWDER FOR CONCENTRATE AND SOLUTION
40 10POWDER FOR SOLUTION
41 1POWDER FOR SOLUTION FOR INFUSION
42 2POWDER FOR SOLUTION FOR INJECTION
43 3POWDER;INTRAVENOUS
44 1POWDER;ORAL
45 1Pegfilgrastim 6Mg 1 Unit Parenteral Use
46 3Powder for infusion fluid, resolution
47 2Powder for injection fluid, resolution
48 1Romiplostim 250Mcg 0.72Ml 1 Units Parenteral Use
49 1Romiplostim 500Mcg 1,2Ml 1 Unit Parenteral Use
50 38SOLUTION
51 11SOLUTION FOR INJECTION
52 13SOLUTION FOR INJECTION IN PRE-FILLED
53 17SOLUTION FOR INJECTION, PRE-FILLED SYRINGE
54 3SOLUTION;INTRAVENOUS
55 1SOLUTION;ORAL
56 1SOLUTION;TOPICAL
57 4SYRINGE
58 3Solution for injection in a pre-filled pen
59 2Solution for injection, solution in pre-filled syringe
60 2TAB
61 5TABLET
62 5TABLET, DELAYED RELEASE;ORAL
63 13TABLET;ORAL
64 2VIAL
65 5VIAL; INTRAVENOUS
66 3VIAL; MULTIDOSE
67 6VIAL; SINGLE-USE
68 6VIAL; SUBCUTANEOUS
69 1VIAL;SINGLE-DOSE
70 18injection
71 67Blank
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01 10.3 MG / ML
02 10.6 MG / ML
03 20.6 mg/ml
04 10.96 MG / ML
05 20.96 mg/ml
06 11 syringe 30,000,000 IU 0.5 ml
07 11 syringe SC 6 mg 0.6 ml with needle shield
08 11 vial 250 mcg groun + solv
09 11 vial 500 mcg groun + solv
10 11 vial SC EV 30,000,000 IU 1 ml
11 11.1G/ML
12 11.1GM/ML
13 210 MICROGRAMS
14 110 mg
15 210 microgram/0.4 mL
16 110,000U/ML
17 3100 MICROGRAMS
18 1100 MILLION PFU / ML
19 2100 microgram/0.5 mL
20 3100MCG/ML
21 1100MG/10ML(10MG/ML)
22 1100MG/4ML (25MG/ML)
23 1100MG/5ML
24 2100MG/VIAL
25 1100UG/0.5ML
26 2100UG/ML
27 2100mcg
28 1100mg/4ml
29 2100mg/5ml
30 1100millionPFU/ml
31 2105MG/1.17ML
32 410MG
33 110MG/2ML (5MG/ML)
34 210MG/ML
35 310MG/VIAL
36 110ML/200MG
37 110mcg
38 110mg
39 110mg and 20mg and 30mg
40 110mg/2ml
41 110µg/0.4ml
42 1120 MG
43 1120 mg
44 2120MG
45 1120MG/1.7ML
46 1120MG/ML
47 1120mg/1.7ml
48 1125mcg
49 2130 MICROGRAMS
50 1130MG/26ML
51 2140 MG
52 4140 mg/ml
53 2140MG/ML
54 1140mg
55 2140mg/ml
56 215 MICROGRAMS
57 2150 MICROGRAM
58 2150 microgram/0.3 mL
59 1150MG
60 1150MG/VIAL
61 1150mcg
62 1150mg
63 1150µg/0.3ml
64 115MG/VIAL
65 115MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
66 21MG
67 11MG/VIAL
68 11millionPFU/ml
69 12 mg (0.05 mL of 40 mg/mL)
70 12% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
71 12,000U/ML
72 12.5MG/0.5ML (2.5MG/0.5ML)
73 12.5mg/0.5ml
74 120 MG/ML
75 220 MICROGRAMS
76 220 microgram/0.5 mL
77 120,000/ML
78 120,000U/2ML
79 1200 MICROGRAM
80 4200MCG/ML
81 2200UG/ML
82 220MG
83 120MG/0.4ML
84 120MG/ML
85 120ML/400MG
86 120mcg
87 120mg
88 120mg/0.2ml
89 120mg/0.4ml
90 120µg/0.5ml
91 1240MG
92 1240MG/2.4ML
93 125 MICROGRAMS
94 2250 MICROGRAM
95 1250 mcg
96 1250MCG/0.5ML; 500MCG/1ML.
97 1250MCG/VIAL
98 1250mcg
99 1250µg/0.5ml
100 125MCG/ML
101 125MG
102 225MG/ML
103 125MG/VIAL
104 225UG/ML
105 126.6MG;800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
106 128 cpr riv 30 mg
107 128 cpr riv 60 mg
108 128 cpr riv 90 mg
109 12MG
110 13,000U/ML
111 130 MG
112 230 MICROGRAMS
113 330 mg
114 230 microgram/0.3 mL
115 3300 MICROGRAMS
116 1300MCG/1ML
117 1300MCG/ML
118 1300MG/30ML(10MG/ML)
119 1300MGC/0.5ML
120 3300mcg
121 1300µg/0.6ml
122 330MG
123 330MG/VIAL
124 130MioU/0.5ml
125 130MioU/ml
126 130mcg
127 530mg
128 130µg/0.3ml
129 1320MG
130 135MCG
131 138.5 MICROGRAM
132 138.5MCG/VIAL
133 138.5mcg
134 13GM/TEASPOONFUL
135 14,000U/ML
136 340 MICROGRAMS
137 240 microgram/0.4 mL
138 140,000U/ML
139 1400MG/16ML (25MG/ML)
140 1400MG/20ML
141 1400mg/16ml
142 1400mg/20ml
143 140MCG/ML
144 140MG/0.8ML
145 240UG/ML
146 240mcg
147 240mg
148 640mg/0.4ml
149 640mg/0.8ml
150 1420MG
151 1420MG/VIAL
152 1440mg
153 445MG/0.5ML
154 1480MCG/0.8ML
155 1480MCG/1.6ML
156 1480mcg
157 148MioU/0.5ml
158 250 G
159 250 microgram/0.5 mL
160 4500 MICROGRAMS
161 1500 mcg
162 1500 µg/0,4ml
163 4500MCG/ML
164 1500MCG/VIAL
165 2500MG
166 2500mcg
167 550MG/ML
168 250mcg
169 15MG
170 15MG/5ML (1MG/ML)
171 25MG/ML
172 15MG/ML (5MG/ML)
173 15ML/100MG
174 15mg/1ml
175 26 MG
176 26 mg
177 460 MG
178 360 MICROGRAMS
179 360 mg
180 260 microgram/0.3 mL
181 2600MCG/ML
182 260MG/ML
183 260MG/VIAL
184 260UG/ML
185 160mcg
186 460mg
187 260mg/ml
188 160µg/0.3ml
189 16MG/0.6ML
190 26mg/0.6ml
191 270MG/ML
192 175MG
193 280 MICROGRAMS
194 280 microgram/0.4 mL
195 280mcg
196 280mg/0.8ml
197 18MG
198 190 MG
199 290 mg
200 290MG/1ML
201 190MG/ML
202 190MG/VIAL
203 190mg
204 1EQ 20MG BASE;375MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
205 1EQ 20MG BASE;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
206 1EQ 25MG BASE
207 1EQ 300MG BASE/PACKET
208 1EQ 30MG BASE
209 1EQ 5MG BASE
210 1EQ 60MG BASE
211 1EQ 7.5MG BASE
212 1EQ 75MG BASE
213 1EQ 75MG BASE/PACKET
214 1EQ 90MG BASE
215 1ONE MILLION PFU / ML
216 68Blank
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01 85Australia
02 57Canada
03 11Italy
04 19Norway
05 27South Africa
06 54Sweden
07 58Switzerland
08 91USA
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : AMGEVITA
Dosage Strength : 50MG/ML
Packaging : 0.8ML
Approval Date :
Application Number : 2459299
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : AMGEVITA
Dosage Strength : 50MG/ML
Packaging : 0.8ML
Approval Date :
Application Number : 2459302
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : AMGEVITA
Dosage Strength : 50MG/ML
Packaging : 0.4ML
Approval Date :
Application Number : 2459310
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : PFS
Brand Name : Amgevita 20mg
Dosage Strength : 20mg
Packaging : 0.4X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : PFP
Brand Name : Amgevita 40mg
Dosage Strength : 40mg
Packaging : 0.8X2mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : PFS
Brand Name : Amgevita 40mg
Dosage Strength : 40mg
Packaging : 0.8X2mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info :
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMJEVITA
Dosage Strength : 20MG/0.4ML
Packaging :
Approval Date :
Application Number : 761024
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMJEVITA
Dosage Strength : 40MG/0.8ML
Packaging :
Approval Date :
Application Number : 761024
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : Switzerland
Dosage Form : Inj Sol
Brand Name : Amgevita
Dosage Strength : 40mg/0.8ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Dosage Form : Inj L?s
Brand Name : Amgevita
Dosage Strength : 40mg/0.4ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
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