01 110 µg of darbepoetin alfa
02 1150 µg of darbepoetin alfa
03 120 µg of darbepoetin alfa
04 130 µg of darbepoetin alfa
05 1300 µg of darbepoetin alfa
06 160 µg of darbepoetin alfa
07 6ADALIMUMAB
08 2ADALIMUMAB-ATTO
09 1AFLIBERCEPT-AYYH
10 7APREMILAST
11 1AVACOPAN
12 16Adalimumabum
13 1Apremilast
14 1Apremilastum
15 1April eve
16 2BEVACIZUMAB
17 2BEVACIZUMAB-AWWB
18 2BLINATUMOMAB
19 2Bevacizumabum
20 1Blinatumomab
21 1Blinatumomabum
22 6CARFILZOMIB
23 3CINACALCET HYDROCHLORIDE
24 2CYSTEAMINE (CYSTEAMINE BITARTRATE)
25 4CYSTEAMINE BITARTRATE
26 4Carfilzomib
27 3Carfilzomibum
28 3Cinacalcet
29 6Cinacalcet Hydrochloride
30 3Cinacalcetum
31 24DARBEPOETIN ALFA
32 4DENOSUMAB
33 1DICLOFENAC SODIUM
34 11Darbepoetinum alfa
35 2Denosumab
36 2Denosumabum
37 1ECULIZUMAB-AEEB
38 7EPOETIN ALFA
39 1ERENUMAB-AOOE
40 2ESOMEPRAZOLE MAGNESIUM; NAPROXEN
41 3ETANERCEPT
42 3ETELCALCETIDE
43 4EVOLOCUMAB
44 3Etelcalcetide
45 2Evolocumabum
46 4Evolokumab
47 1FAMOTIDINE; IBUPROFEN
48 16FILGRASTIM
49 3Filgrastim
50 3Filgrastimum ADNr
51 2GLYCEROL PHENYLBUTYRATE
52 1INEBILIZUMAB
53 1INFLIXIMAB
54 1INFLIXIMAB-AXXQ
55 1INTERFERON GAMMA-1B
56 1IVABRADINE
57 2IVABRADINE HYDROCHLORIDE
58 1LEVOFLOXACIN (LEVOFLOXACIN HEMIHYDRATE)
59 1LEVOMEPROMAZINE
60 1OXALIPLATIN
61 2PAMIDRONATE DISODIUM
62 5PANITUMUMAB
63 2PEGFILGRASTIM
64 1PEGLOTICASE
65 3PREDNISONE
66 1Panitumumab
67 2Panitumumabum
68 1Pegfilgrastim
69 1Pegfilgrastimum
70 1RITUXIMAB-ARRX
71 3ROMIPLOSTIM
72 1ROMOSOZUMAB
73 1ROMOSOZUMAB-AQQG
74 4Romiplostim
75 2SODIUM PHENYLBUTYRATE
76 4SOTORASIB
77 4Su 5416
78 2TARLATAMAB-DLLE
79 1TEPROTUMUMAB-TRBW
80 2THIOTEPA
81 2TRASTUZUMAB
82 2TRASTUZUMAB-ANNS
83 2Talimogenum laherparepvecum
84 2Trastuzumabum
85 4USTEKINUMAB
86 3USTEKINUMAB-AUUB
87 2apremilast
88 4bevacizumab
89 9blinatumomab
90 18carfilzomib
91 2cinacalcet
92 3cinakalcethydroklorid
93 66darbepoetin alfa
94 6denosumab
95 4evolocumab
96 2evolokumab
97 3filgrastim
98 1karfilzomib
99 9panitumumab
100 2pegfilgrastim
101 8romiplostim
102 2romosozumab
103 2talimogen laherparepvek
01 32AMGEN
02 47AMGEN CANADA INC
03 8AMGEN EUROPE B.V.
04 3AMGEN EUROPE BV
05 27AMGEN INC
06 83Amgen Australia Pty Limited
07 21Amgen Europe B.V.
08 52Amgen Europe BV
09 27Amgen South Africa (Pty) Ltd
10 58Amgen Switzerland AG
11 1CHEMOCENTRYX
12 11HORIZON
13 1HORIZON PHARMA
14 3HORIZON THERAP US
15 1HORIZON THERAPEUTICS IRELAND
16 6HORIZON THERAPEUTICS IRELAND DAC
17 5IMMUNEX
18 1IMMUNEX CORPORATION
19 3KAI PHARMS INC
20 2MN PHARMS
21 1MUSTAFA NEVSAT IIAC SANAYII A.S.
22 3ONYX PHARMS AMGEN
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 8POWDER 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 36SOLUTION
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 65Blank
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 210MG/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 11millionPFU/ml
68 12 mg (0.05 mL of 40 mg/mL)
69 12% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
70 12,000U/ML
71 12.5MG/0.5ML (2.5MG/0.5ML)
72 12.5mg/0.5ml
73 120 MG/ML
74 220 MICROGRAMS
75 220 microgram/0.5 mL
76 120,000/ML
77 120,000U/2ML
78 1200 MICROGRAM
79 4200MCG/ML
80 2200UG/ML
81 320MG
82 120MG/0.4ML
83 120MG/ML
84 120ML/400MG
85 120mcg
86 120mg/0.2ml
87 120mg/0.4ml
88 120µg/0.5ml
89 1240MG
90 1240MG/2.4ML
91 125 MICROGRAMS
92 2250 MICROGRAM
93 1250 mcg
94 1250MCG/0.5ML; 500MCG/1ML.
95 1250MCG/VIAL
96 1250mcg
97 1250µg/0.5ml
98 125MCG/ML
99 125MG
100 225MG/ML
101 125MG/VIAL
102 225UG/ML
103 126.6MG;800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
104 128 cpr riv 30 mg
105 128 cpr riv 60 mg
106 128 cpr riv 90 mg
107 12MG
108 13,000U/ML
109 130 MG
110 230 MICROGRAMS
111 330 mg
112 230 microgram/0.3 mL
113 3300 MICROGRAMS
114 1300MCG/1ML
115 1300MCG/ML
116 1300MG/30ML(10MG/ML)
117 1300MGC/0.5ML
118 3300mcg
119 1300µg/0.6ml
120 330MG
121 330MG/VIAL
122 130MioU/0.5ml
123 130MioU/ml
124 130mcg
125 530mg
126 130µg/0.3ml
127 1320MG
128 135MCG
129 138.5 MICROGRAM
130 138.5MCG/VIAL
131 138.5mcg
132 13GM/TEASPOONFUL
133 14,000U/ML
134 340 MICROGRAMS
135 240 microgram/0.4 mL
136 140,000U/ML
137 1400MG/16ML (25MG/ML)
138 1400MG/20ML
139 1400mg/16ml
140 1400mg/20ml
141 140MCG/ML
142 240MG
143 140MG/0.8ML
144 240UG/ML
145 240mcg
146 640mg/0.4ml
147 640mg/0.8ml
148 1420MG
149 1420MG/VIAL
150 1440mg
151 345MG/0.5ML
152 1480MCG/0.8ML
153 1480MCG/1.6ML
154 1480mcg
155 148MioU/0.5ml
156 250 G
157 250 microgram/0.5 mL
158 4500 MICROGRAMS
159 1500 mcg
160 1500 µg/0,4ml
161 4500MCG/ML
162 1500MCG/VIAL
163 2500MG
164 2500mcg
165 550MG/ML
166 250mcg
167 15MG
168 15MG/5ML (1MG/ML)
169 25MG/ML
170 15MG/ML (5MG/ML)
171 15ML/100MG
172 15mg/1ml
173 26 MG
174 26 mg
175 460 MG
176 360 MICROGRAMS
177 360 mg
178 260 microgram/0.3 mL
179 2600MCG/ML
180 260MG/ML
181 260MG/VIAL
182 260UG/ML
183 160mcg
184 460mg
185 260mg/ml
186 160µg/0.3ml
187 16MG/0.6ML
188 26mg/0.6ml
189 270MG/ML
190 175MG
191 280 MICROGRAMS
192 280 microgram/0.4 mL
193 280mcg
194 280mg/0.8ml
195 18MG
196 190 MG
197 290 mg
198 190MG/1ML
199 190MG/ML
200 190MG/VIAL
201 190mg
202 1EQ 20MG BASE;375MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
203 1EQ 20MG BASE;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
204 1EQ 25MG BASE
205 1EQ 300MG BASE/PACKET
206 1EQ 30MG BASE
207 1EQ 5MG BASE
208 1EQ 60MG BASE
209 1EQ 7.5MG BASE
210 1EQ 75MG BASE
211 1EQ 75MG BASE/PACKET
212 1EQ 90MG BASE
213 1ONE MILLION PFU / ML
214 66Blank
01 83Australia
02 53Canada
03 11Italy
04 19Norway
05 27South Africa
06 54Sweden
07 58Switzerland
08 91USA
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Aranesp 10µg
Dosage Strength : 10µg/0.4ml
Packaging : 1X1µg/0.4ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Aranesp 150µg
Dosage Strength : 150µg/0.3ml
Packaging : 1X1µg/0.3ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Aranesp 20µg
Dosage Strength : 20µg/0.5ml
Packaging : 1X1µg/0.5ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Aranesp 30µg
Dosage Strength : 30µg/0.3ml
Packaging : 1X1µg/0.3ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Aranesp 300µg
Dosage Strength : 300µg/0.6ml
Packaging : 1X1µg/0.6ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Aranesp 60µg
Dosage Strength : 60µg/0.3ml
Packaging : 1X1µg/0.3ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info :
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : AMGEVITA
Dosage Strength : 50MG/ML
Packaging : 0.8ML
Approval Date :
Application Number : 2459299
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : AMGEVITA
Dosage Strength : 50MG/ML
Packaging : 0.8ML
Approval Date :
Application Number : 2459302
Regulatory Info :
Registration Country : Canada
Regulatory Info : Generic
Registration Country : South Africa
Dosage Form : PFS
Brand Name : AMGEVITA 20MG
Dosage Strength : 20MG
Packaging : 0.4X1MG
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Dosage Form : PFS
Brand Name : AMGEVITA 40MG
Dosage Strength : 40MG
Packaging : 0.8X2MG
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
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