Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
01 1Octavius Pharma Pvt. Ltd
02 2Pharmathen SA
03 1AGIPS FARMACEUTICI Srl
04 1ALMUS Srl
05 2ANGITA PHARMA INC.
06 2Abdi Ibrahim
07 6Accord healthcare
08 8Actavis Inc
09 2Alphapharm PTY Ltd
10 9Apotex Inc
11 2Auro Pharma Inc
12 5Aurobindo Pharma Limited
13 1BRUNO FARMACEUTICI SpA
14 2Blue Fish Solvay AB
15 9Chartwell Pharmaceuticals llc
16 5Cipla
17 1DOC Generici
18 1EG SpA
19 1EPIFARMA Srl
20 1FG Srl
21 1Farm Agon
22 1Flagship Biotech International Pvt. Ltd
23 1Halewood Laboratories Pvt. Ltd
24 4Hangzhou Minsheng Binjiang Pharmaceutical CO., Ltd
25 1Hikma Pharmaceuticals
26 1IBN Savio
27 1IFA SA Laboratories
28 1IST.CHIM.INTERNAZ. RENDE Srl
29 5Impax Laboratories
30 1Infugen Pharma
31 3Intas Pharmaceuticals
32 4Ipca Laboratories
33 1JAMP PHARMA
34 4Jubilant Cadista Pharmaceuticals
35 1Kusum Healthcare Pvt Ltd
36 1LABORATOIRE RIVA INC.
37 2Laboratoires Teriak TN
38 2Laboratorios Alter
39 1Loxim Industries
40 1MANTRA PHARMA INC
41 1MINT PHARMACEUTICALS INC
42 1MS Pharma
43 11Merck & Co
44 2Myungmoon Pharm. Co., LTD.
45 1NEAPHARMA Srl
46 4NEOPHARMED GENTILI Srl
47 1Nora Pharma
48 1Novitium Pharma LLC
49 1ORGANON CANADA INC.
50 7Organon
51 1Organon South Africa (Pty) Ltd
52 1PRO DOC LIMITEE
53 1Pensa Pharma
54 1Pharmacare Premium
55 3Pharmascience Inc.
56 1Radius Health
57 1Ratiopharm GmbH
58 4Rising Pharmaceuticals Inc
59 4S.F.GROUP Srl
60 1SANIS HEALTH INC
61 2SIGMA TAU
62 1SIVEM PHARMACEUTICALS ULC
63 1SO.SE.PHARM Srl
64 6Sandoz B2B
65 6Sun Pharmaceutical Industries Limited
66 1TECNIGEN Srl
67 8Teva Pharmaceutical Industries
68 7Viatris
69 2WAGNER PHARMACEUTICALS PTY LTD
70 1World Medicine
71 1XL Laboratories Private Limited
72 1Yangtze River Pharmaceutical Group
73 1Zentiva
74 6Zim Laboratories
75 40Blank
01 4Alendronic Acid 10Mg 14 Joined' Oral Use
02 1Alendronic Acid 70Mg 100Ml 4 Units' Oral Use
03 2Alendronic Acid 70Mg 12 Combined Oral Use
04 29Alendronic Acid 70Mg 4 Units' Oral Use
05 3Alendronic Acid+Cholecalciferol 70Mg + 2.800Iu 4 Units' Oral Use
06 4Alendronic Acid+Cholecalciferol 70Mg + 5.600Iu 4 Units' Oral Use
07 15Antic-calc Tablet
08 2Antic-calc Tablet, Film Coated
09 2DC Granules
10 5DC Granules and Tablets
11 2Film Coated Tablet
12 3SOLUTION;ORAL
13 3TAB
14 34TABLET
15 1TABLET, EFFERVESCENT;ORAL
16 60TABLET;ORAL
17 53Tablet
18 8tablet
01 31DISCN
02 2EU Approved
03 10Generic
04 2Generic B.E study
05 1Originator
06 24Prescription
07 33RX
08 128Blank
01 14 Bifoal Weekly 70Mg Film-Coated Tablets Efg
02 14 Lefosan Weekly 70Mg Tablets Efg
03 14 Semandrol Weekly 70Mg Tablets Efg
04 3ACH-ALENDRONATE
05 1AG-ALENDRONATE
06 1AG-ALENDRONATE SODIUM
07 1ALENDRA
08 2ALENDRONATE
09 55ALENDRONATE SODIUM
10 1ALENDRONATE-70
11 2ALENDRONATE-WGR
12 1ALENDROXL
13 1APO-ALENDRONATE
14 2APO-ALENDRONATE/VITAMIN D3
15 2APO-Alendronate
16 2AURO-ALENDRONATE
17 1Ac Alendr Liderfarm 70Mg 4 Weekly Com Rec Pel Efg
18 1Ac Alendronico/Cholecalciferol Weekly Sandoz 70Mg/5,600Iu 4 Comp Efg
19 1Acid Alendronico Teva 70Mg 4 Comprimid Efg
20 2Adronat
21 2Adrovance
22 1Adrovance 70Mg/2800Iu 4 Tablets
23 1Adrovance 70Mg/5600Iu 4 Tablets
24 4Alendronat Arrow
25 2Alendronat Blue Fish
26 4Alendronat Mylan
27 2Alendronat Sandoz
28 2Alendronat Teva
29 11Alendronate
30 1Alendronate And Cholecalciferol
31 1Alendronate Ranbaxy Veckotablett
32 2Alendronate Sandoz
33 1Alendronate Sodium
34 1Alendronate Teva Veckotablett
35 5Alendronic Acid
36 1Alendronico Acid/Cholecalciferol Ratiopharm 70 Mg/2800Iu 4 Compri
37 1Alendronico Acid/Cholecalciferol Ratiopharm 70 Mg/5,600Iu 4 Compr
38 1Alendronico/Cholecalciferol Tevagen Acid 70Mg/2800Iu 4 Tablets
39 1Alendronico/Cholecalciferol Tevagen Acid 70Mg/5,600Iu 4 Tablets
40 1Alenic
41 1Apotex Alendronico Acid 70Mg 4 Tablets Efg
42 1Aston
43 1Aurovitas Weekly Alendronico Acid 70Mg 4 Recub Comprim Efg
44 1BINOSTO
45 1Bonasol
46 1Bonpil
47 1Bonpil Plus D
48 1Combix Weekly Alendronico Acid 70Mg 4 Recubier Comprimid Peli Efg
49 1Davur Weekly Alendronico Acid 70Mg 4 Comprim Efg
50 1Developed Weekly 70Mg 4 Tablets Efg
51 1Doryx
52 1Dralen
53 2Dronal
54 7FOSAMAX
55 2FOSAMAX PLUS D
56 2Famax
57 2Favance
58 2Fonat
59 2Fosalen
60 3Fosamax
61 1Fosavance 5 600
62 2Fosavance 70Mg/2800Iu 4 Tablets
63 2Fosavance 70Mg/5600Iu 4 Tablets
64 2Genalen
65 1Glamor
66 1JAMP ALENDRONATE SODIUM
67 1Kernpharma Weekly Alendronico Acid 70Mg 4 Co Efg
68 1Korhispana Weekly Alendronico Acid 70Mg 4 Co Efg
69 1Ls
70 1M-ALENDRONATE
71 1MINT-ALENDRONATE
72 1Mylan Weekly Alendronico Acid 70Mg 4 Tablets Efg
73 1NRA-ALENDRONATE
74 1Neadrale
75 1Nofrattil
76 1Ostena 10
77 1Ostena 70
78 1PMS-ALENDRONATE
79 2PMS-ALENDRONATE-FC
80 1Pdron
81 1Pharmagenus Weekly Alendronico Acid 70Mg 4 C Efg
82 1Qualigen Weekly Alendronico Acid 70Mg 4 Comp Efg
83 1RIVA-ALENDRONATE FC
84 1Realen
85 1SANDOZ ALENDRONATE
86 1TEVA-ALENDRONATE
87 1Tecnigen Weekly Alendronico Acid 70Mg 4 Comp Efg
88 1Teum
89 2Vantavo
90 1Weekly Alendronico Acid 4 Cinfamed 70Mg Tablets Efg
91 1Weekly Alendronico Acid Alter Generic 70Mg 4 Com Rec Pel Efg
92 1Weekly Alendronico Acid Ratio 70Mg 4 Tablets Efg
93 1Weekly Alendronico Acid Stada 70Mg 4 Comprim Efg
94 1Weekly Alendronico Almus Acid 70Mg 4 Recub Comprimid Film Efg
95 1Weekly Alendronico Aurobindo Acid 70Mg 4 Tablets Efg
96 1Weekly Alendronico Mabo Acid 70Mg 4 Comprimi Efg
97 1Weekly Alendronico Normon Acid 70Mg 4 Compr Efg
98 1Weekly Alendronico Ranbaxy Acid 70Mg 4 Comprimidosefg
99 1Weekly Alendronico Sandoz Acid 70Mg 4 Tablets Efg
100 1Weekly Alendronico Vir Acid 70Mg 4 Comprimid Efg
101 1Weekly Fosamax 70Mg 4 Tablets
102 1Weekly Think Alendronico Acid 70Mg 4 Tablets Efg
103 1alendronate Teva
104 22Blank
01 8Australia
02 1Bolivia
03 24Canada
04 1China
05 2Greece
06 17India
07 43Italy
08 1Jordan
09 17Norway
10 3South Africa
11 2South Korea
12 40Spain
13 3Sweden
14 2Tunisia
15 3Turkey
16 64USA
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Brand Name : Alendronate Sodium
Dosage Form : DC Granules
Dosage Strength : 70MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Pharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.
Regulatory Info : EU Approved
Registration Country : Greece
Alendronate Sodium; Vitamin D3
Brand Name :
Dosage Form : Tablet
Dosage Strength : 70MG; 2800IU
Packaging :
Approval Date :
Application Number :
Regulatory Info : EU Approved
Registration Country : Greece
Pharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.
Regulatory Info : EU Approved
Registration Country : Greece
Alendronate Sodium; Vitamin D3
Brand Name :
Dosage Form : Tablet
Dosage Strength : 70MG; 5600IU
Packaging :
Approval Date :
Application Number :
Regulatory Info : EU Approved
Registration Country : Greece
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2009-04-22
Application Number : 75871
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2009-04-22
Application Number : 75871
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 40MG BASE
Packaging :
Approval Date : 2009-04-22
Application Number : 75871
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 35MG BASE
Packaging :
Approval Date : 2009-04-22
Application Number : 75871
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 70MG BASE
Packaging :
Approval Date : 2009-04-22
Application Number : 75871
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2008-08-04
Application Number : 76768
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2008-08-04
Application Number : 76768
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 35MG BASE
Packaging :
Approval Date : 2008-08-04
Application Number : 76768
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2008-02-06
Application Number : 75710
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2008-02-06
Application Number : 75710
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 35MG BASE
Packaging :
Approval Date : 2008-02-06
Application Number : 75710
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 40MG BASE
Packaging :
Approval Date : 2008-02-06
Application Number : 75710
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 70MG BASE
Packaging :
Approval Date : 2008-02-06
Application Number : 75710
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FOSAMAX
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 70MG BASE/75ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2003-09-17
Application Number : 21575
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FOSAMAX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1995-09-29
Application Number : 20560
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FOSAMAX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1995-09-29
Application Number : 20560
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FOSAMAX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1997-04-25
Application Number : 20560
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FOSAMAX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 35MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2000-10-20
Application Number : 20560
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FOSAMAX
Dosage Form : TABLET;ORAL
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
Brand Name : FOSAMAX PLUS D
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 70MG BASE;2,800 IU
Packaging :
Approval Date : 2005-04-07
Application Number : 21762
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ALENDRONATE SODIUM; CHOLECALCIFEROL
Brand Name : FOSAMAX PLUS D
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 70MG BASE;5,600 IU
Packaging :
Approval Date : 2007-04-26
Application Number : 21762
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2008-08-04
Application Number : 76584
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2008-08-04
Application Number : 76584
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 35MG BASE
Packaging :
Approval Date : 2008-08-04
Application Number : 76584
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 70MG BASE
Packaging :
Approval Date : 2008-08-04
Application Number : 76584
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 70MG BASE
Packaging :
Approval Date : 2008-02-06
Application Number : 76184
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALENDRONATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 35MG BASE
Packaging :
Approval Date : 2008-08-04
Application Number : 76184
Regulatory Info : DISCN
Registration Country : USA
