01 5ALENDRONATE SODIUM
02 2ALENDRONATE SODIUM; CHOLECALCIFEROL
03 4ATORVASTATIN CALCIUM; EZETIMIBE
04 4Acidum alendronicum; cholecalciferol (vitamin D3)
05 3Alendronic acid
06 6Alendronic acid; Cholecalciferol
07 6Asenapine
08 1BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE
09 3BETAMETHASONE DIPROPIONATE
10 1BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE
11 2Betamethasone; Clotrimazolum; Gentamicinum
12 3Betamethasone; Salicylic Acid
13 4Betamethasonum
14 2Betamethasonum; Gentamicinum
15 5CARBIDOPA; LEVODOPA
16 1CLINDAMYCIN PHOSPHATE
17 2Corifollitropin alfa
18 3DESLORATADINE
19 2DESLORATADINE; PSEUDOEPHEDRINE SULFATE
20 7Desloratadine
21 1Desogestrel
22 2Desogestrel, Ethinylestradiol
23 1ETHINYL ESTRADIOL; ETONOGESTREL
24 2ETONOGESTREL
25 1EZETIMIBE
26 4EZETIMIBE; SIMVASTATIN
27 2Enalapril
28 2Enalapril; Hydrochlorothiazide
29 2Estradiol Valerate; Medroxyprogesterone Acetate
30 1Estriol
31 6Ethinyl Estradiol; Desogestrel
32 2Etonogestrel
33 1Etonogestrel; Ethinyl Estradiol
34 3Etoricoxib
35 3Etoricoxibum
36 5Ezetimibe
37 3Ezetimibe; Simvastatin
38 8Ezetimibum; Atorvastatinum
39 2FINASTERIDE
40 3FORMOTEROL FUMARATE; MOMETASONE FUROATE
41 2Felbamatum
42 5Finasteride
43 12Follitropin beta
44 3Follitropinum beta ADNr
45 1GANIRELIX ACETATE
46 2Ganirelix
47 2Gonadorelin
48 3HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
49 54Infliximab
50 4Karbidopa, Levodopa
51 3LOSARTAN POTASSIUM
52 2Levodopa; Carbidopa
53 4Levodopum; Carbidopum
54 3Losartan
55 2Losartan; Hydrochlorothiazide
56 3Losartankalium
57 3Losartankalium, Hydroklortiazid
58 4Losartanum kalicum
59 6Losartanum kalium; Hydrochlorothiazide
60 6MIRTAZAPINE
61 10MOMETASONE FUROATE
62 4MONTELUKAST SODIUM
63 15Mirtazapine
64 2Mometasone furoate monohydrate
65 7Mometasone-17 furoase
66 20Montelukast
67 2Nandrolone
68 2Orgalutran
69 4RIZATRIPTAN BENZOATE
70 2ROCURONIUM BROMIDE
71 12Rizatriptan
72 6Rizatriptanbenzoat
73 5SIMVASTATIN
74 7Simvastatin
75 6Simvastatinum; Ezetimibum
76 1Tibolon
77 2Tibolone
78 2Tibolonum
79 2asenapinmaleat
80 2betamethasone acetate + betamethasone sodium phosphate
81 2chorionic gonadotropin (human urine)
82 3mirtazapine
83 1tibolone
01 7NV ORGANON
02 6NV Organon
03 29NV Organon - Kloosterstraat
04 2NV Organon,
05 54ORGANON
06 35ORGANON ITALIA SRL
07 17ORGANON ITALIA SpA
08 17ORGANON LLC
09 8ORGANON N.V.
10 5ORGANON USA ORGANON
11 106Organon GmbH
12 77Organon Pharma Pty Ltd
01 6AEROSOL, METERED;INHALATION
02 1Asenapina 10Mg 60 Units Sublingual Use
03 1Asenapina 5Mg 60 Units Sublingual Use
04 1CREAM, AUGMENTED;TOPICAL
05 3CREAM;TOPICAL
06 10Chewable Tablets
07 1Chorionic Gonadotropin 5.000Iu 1 Unit Parenteral Use
08 2Compresse Rivestite Con Film
09 3Cream
10 3Creme
11 1Depot tablet
12 2Film Tablets
13 34Film-Coated Tablets
14 8Filmtabl
15 1Filmtable
16 1GEL;VAGINAL
17 1GRANULE;ORAL
18 2Gran
19 2Granules
20 1HARD CAPSULES
21 2IMPLANT;IMPLANTATION
22 2INJECTABLE;INJECTION
23 1Implant
24 5Inj L?s
25 1Inj L?s Einwegspr
26 2Injection; Injection
27 1LOTION, AUGMENTED;TOPICAL
28 1LOTION;TOPICAL
29 6Melting tablet
30 1Mirtazapine 15Mg/Ml 66Ml Oral Use
31 1Mirtazapine 30Mg 30 Joined' Oral Use
32 1Mixture, solution
33 2Modified Release Tablets
34 1Nasal Spray
35 2Nasal spray, suspension
36 1OINTMENT, AUGMENTED;TOPICAL
37 1OINTMENT;TOPICAL
38 3ORODISPERSIBLE TABLET
39 3Ointment
40 2Oral
41 4Orodispersible Tablets
42 2POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
43 2POWDER;INHALATION
44 1RING;VAGINAL
45 1Rocuronium 100Mg 10Ml 10 Units Parenteral Use
46 1Rocuronium 50Mg 5Ml 10 Units Parenteral Use
47 1SPRAY, METERED;NASAL
48 2SUBLINGUAL TABLET
49 1Salbe
50 4Solution
51 2Subling Tabl
52 1Susp
53 2TABLET, CHEWABLE;ORAL
54 4TABLET, EXTENDED RELEASE;ORAL
55 7TABLET, ORALLY DISINTEGRATING;ORAL
56 39TABLET;ORAL
57 26Tabl
58 19Tablet
59 9Tablet, film-coated
60 18Tablets
61 1Tablets 3 Tablets In Blister
62 1Tibolone 2,5Mg 30 Joined' Oral Use
63 1injection
64 2tablet
65 89Blank
01 10.005MG/INH;0.05MG/INH
02 10.005MG/INH;0.1MG/INH
03 10.005MG/INH;0.2MG/INH
04 10.015MG/24HR;0.12MG/24HR
05 10.05%
06 10.05MG/INH
07 10.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 10.1%
09 30.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 10.10MG/INH
11 10.11MG/INH
12 10.20MG/INH
13 10.22MG/INH
14 10.5 mg/ml
15 11 Ampoule Im 25 Mg 1 Ml
16 11 Syringe 0.25 Mg 0.5 Ml
17 11 Syringe Im 50 Mg 1 Ml
18 11 System Vaginal Release
19 11 vial IM 5,000 IU + 1 ampoule solv 1 ml
20 11.25 MG
21 110 MG
22 110 VIALS EV 10 ml 10 mg/ml
23 110 VIALS EV 5 ml 10 mg/ml
24 1110 mg
25 110 mg/10 mg
26 110 mg/20 mg
27 110 mg/40 mg
28 410/10mg
29 410/20mg
30 410/40mg
31 210/80mg
32 2100 mg
33 1100 mg + 25 mg
34 1100+25 mg
35 2100/12.5
36 2100/25
37 1100MG
38 2100mg
39 1100mg/12.5mg
40 1100mg/25mg
41 210MG
42 110MG;100MG
43 110MG;10MG
44 110MG;20MG
45 110MG;40MG
46 110MG;80MG
47 1710mg
48 111 Cpr White + 10 Heavenly Cpr
49 212,5 mg/50 mg
50 112.5 mg
51 112.5MG;100MG
52 112.5MG;50MG
53 1120 mg
54 1126 Cpr 0.15 Mg + 0.02 Mg
55 115 mg
56 1150 microg/20 microg
57 1150 microg/30 microg
58 11500 IU
59 315MG
60 215mg
61 11MG
62 61mg/g
63 22.5 mg
64 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
65 12.5MG;120MG
66 22.5mg
67 120 Cpr 1 Mg
68 220 mg
69 120 mg+12.5 mg
70 120 mg/6 mg
71 1200 mg+50 mg
72 120MG
73 220mg
74 121 Cpr 0.15 Mg + 0.02 Mg
75 225 mg/100 mg
76 1250 microgram/0.5 mL
77 1250MCG/0.5ML
78 125MG
79 225MG;100MG
80 125MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
81 125MG;250MG
82 225mg/100mg
83 225mg/250mg
84 128 Cpr Riv 0.075 Mg
85 13 Ampoules Im 1,500 Iu + 3 Ampoules 1 Ml
86 13 Blist 7 Cpr Blue + 15 White Cpr
87 130 CPR 2.5 mg
88 130 MG
89 130 cpr orodispers 30 mg
90 330 mg
91 230MG
92 630mg
93 133 Cpr White + 30 Heavenly Cpr
94 13MG/ML;EQ 3MG BASE/ML
95 34 mg
96 140 mg
97 140MG
98 240mg
99 145 MG
100 145 mg
101 145MG
102 145MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
103 64mg
104 15 MG
105 15 Syringes 0.25 Mg 0.5 Ml
106 95 mg
107 25.7MG; 3.9MG
108 350 mg
109 150 mg/12.5 mg
110 250 microg/dose
111 150+12.5 mg
112 250/12.5
113 15000 IU
114 150MG
115 150MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
116 150mcg
117 250mg
118 35MG
119 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
120 15MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
121 125mg
122 16 Cpr Orodispers 15 Mg
123 160 mg
124 160 sublingual CPR 5 mg
125 160 sublingual cpr 10 mg
126 1600mg
127 1600mg/5ml
128 260mg
129 163 Cpr 0.15 Mg + 0.02 Mg
130 268 mg
131 268MG/IMPLANT
132 17 Cpr Blue + 15 White Cpr
133 17 Yellow Cpr + 7 Red Cpr + 7 White Cpr
134 170 mg
135 370 mg/2,800 iu
136 270 mg/5600
137 170 mg/5600 iu
138 270/2800
139 270/5600
140 270mg
141 180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
142 190 mg
143 1EQ 0.05% BASE
144 2EQ 0.05% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
145 1EQ 0.05% BASE;1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
146 3EQ 10MG BASE
147 1EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
148 1EQ 10MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
149 1EQ 2% BASE
150 1EQ 20MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
151 1EQ 35MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
152 1EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
153 1EQ 40MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
154 1EQ 4MG BASE
155 1EQ 4MG BASE/PACKET
156 1EQ 5MG BASE
157 3EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
158 1EQ 70MG BASE
159 1EQ 70MG BASE;2,800 IU
160 1EQ 70MG BASE;5,600 IU
161 1EQ 80MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
162 1os soluz 66 ml 15 mg/ml
163 84Blank
01 77Australia
02 67Italy
03 29Norway
04 8Sweden
05 106Switzerland
06 76USA
Regulatory Info :
Registration Country : Switzerland
Acidum alendronicum; cholecalciferol (vitamin D3)
Dosage Form : Tabl
Brand Name : Fosavance weekly tablets
Dosage Strength : 70/2800
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Acidum alendronicum; cholecalciferol (vitamin D3)
Dosage Form : Tabl
Brand Name : Fosavance weekly tablets
Dosage Strength : 70/2800
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Acidum alendronicum; cholecalciferol (vitamin D3)
Dosage Form : Tabl
Brand Name : Fosavance weekly tablets
Dosage Strength : 70/5600
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Acidum alendronicum; cholecalciferol (vitamin D3)
Dosage Form : Tabl
Brand Name : Fosavance weekly tablets
Dosage Strength : 70/5600
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FOSAMAX
Dosage Strength : EQ 10MG BASE **Federal...
Packaging :
Approval Date : 1995-09-29
Application Number : 20560
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FOSAMAX
Dosage Strength : EQ 40MG BASE **Federal...
Packaging :
Approval Date : 1995-09-29
Application Number : 20560
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FOSAMAX
Dosage Strength : EQ 5MG BASE **Federal ...
Packaging :
Approval Date : 1997-04-25
Application Number : 20560
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FOSAMAX
Dosage Strength : EQ 35MG BASE **Federal...
Packaging :
Approval Date : 2000-10-20
Application Number : 20560
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FOSAMAX
Dosage Strength : EQ 70MG BASE
Packaging :
Approval Date : 2000-10-20
Application Number : 20560
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ALENDRONATE SODIUM; CHOLECALCIFEROL
Dosage Form : TABLET;ORAL
Brand Name : FOSAMAX PLUS D
Dosage Strength : EQ 70MG BASE;2,800 IU
Packaging :
Approval Date : 2005-04-07
Application Number : 21762
Regulatory Info : RX
Registration Country : USA
Organon is a supplier offers 3 products (APIs, Excipients or Intermediates).
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