01 4BUPRENORPHINE
02 8BUPRENORPHINE (BUPRENORPHINE HYDROCHLORIDE)
03 3BUPRENORPHINE HYDROCHLORIDE
04 6BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
05 11Buprenorphine
06 2Buprenorphine; Naloxone
07 3Buprenorphinum
08 1NALMEFENE HYDROCHLORIDE
09 4NALOXONE (NALOXONE HYDROCHLORIDE DIHYDRATE)
10 4NALOXONE (NALOXONE HYDROCHLORIDE)
11 2RISPERIDONE
12 3Several substances refer to content
13 5buprenorphine
14 2buprenorphine + naloxone
15 6buprenorphine hydrochloride
01 14INDIVIOR
02 24INDIVIOR UK LIMITED
03 7Indivior Pty Ltd
04 3Indivior Switzerland AG
05 9Indivior UK Limited
06 7Indivior UK Limited (1)
01 1Buprenorphine 0,2Mg 10 Units Oral Use
02 1Buprenorphine 0,3Mg 1Ml 5 Units Parenteral Use
03 1Buprenorphine 2Mg 7 Units' Oral Use
04 1Buprenorphine 8Mg 7 Units' Oral Use
05 1Buprenorphine+Naloxone 8+2Mg 7 Units' Oral Use
06 1Buprenorphine+Naloxone+0,52 Mg 7 Units' Oral Use
07 8FILM, SOLUBLE
08 4FILM;BUCCAL, SUBLINGUAL
09 2FOR SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS
10 2Film; Film
11 1INJECTABLE;INJECTION
12 1Injection fluid, resolution
13 2SOLUTION (EXTENDED RELEASE)
14 1SOLUTION FOR INJECTION
15 2SOLUTION, EXTENDED RELEASE;SUBCUTANEOUS
16 1SPRAY;NASAL
17 8SUBLINGUAL TABLET
18 3Subling Tabl
19 6Sublingvaltablett
20 8TABLET
21 4TABLET;SUBLINGUAL
22 5Blank
01 10.2 MG
02 10.2 mg
03 10.3 MG / ML
04 10.3 mg/ml
05 20.4 MG
06 10.4 mg
07 10.4mg
08 20.5MG
09 110 sublingual cpr 0.2 mg
10 1100MG/0.5ML
11 1100MG/0.5ML (100MG/0.5ML)
12 1120MG
13 212MG
14 116 MG / 4 MG
15 116MG
16 11MG
17 12 MG
18 12 MG / 0.5 MG
19 12 mg
20 12 mg/0.5 mg
21 42MG
22 12MG; 0.5MG
23 12mg
24 1300MG/1.5ML
25 1300MG/1.5ML (200MG/ML)
26 23MG
27 24MG
28 15 VIALS IM EV 0.3 mg 1 ml
29 17 sublingual CPR 2 mg
30 17 sublingual CPR 2 mg + 0.5 mg
31 17 sublingual CPR 8 mg
32 17 sublingual CPR 8 mg + 2 mg
33 18 MG
34 18 MG / 2 MG
35 18 mg
36 18 mg/2 mg
37 28MG
38 18MG; 2MG
39 18mg
40 190MG
41 1EQ 0.3MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
42 1EQ 12MG BASE;EQ 3MG BASE
43 1EQ 2.7MG BASE/SPRAY
44 1EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
45 1EQ 2MG BASE;EQ 0.5MG BASE
46 1EQ 2MG BASE;EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
47 1EQ 4MG BASE;EQ 1MG BASE
48 1EQ 8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
49 1EQ 8MG BASE;EQ 2MG BASE
50 1EQ 8MG BASE;EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
51 5Blank
01 7Australia
02 18Canada
03 6Italy
04 7Norway
05 9Sweden
06 3Switzerland
07 14USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION, EXTENDED RELEA...
Brand Name : SUBLOCADE
Dosage Strength : 100MG/0.5ML (100MG/0.5...
Packaging :
Approval Date : 2017-11-30
Application Number : 209819
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Dosage Form : Buprenorphine 0,2Mg 10 U...
Brand Name : Teesic
Dosage Strength : 10 sublingual cpr 0.2 ...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Buprenorphine 8Mg 7 Unit...
Brand Name : Subutex
Dosage Strength : 7 sublingual CPR 8 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Dosage Form : Sublingvaltablett
Brand Name : Suboxone
Dosage Strength : 8 mg/2 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Sublingvaltablett
Brand Name : Subutex
Dosage Strength : 2 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Sublingvaltablett
Brand Name : Temgesic
Dosage Strength : 0.2 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Sublingvaltablett
Brand Name : Temgesic
Dosage Strength : 0.4 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : SOLUTION (EXTENDED RELEA...
Brand Name : SUBLOCADE
Dosage Strength : 300MG/1.5ML
Packaging : 1.5ML
Approval Date :
Application Number : 2483092
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info :
Registration Country : Australia
Dosage Form :
Brand Name : Subutex
Dosage Strength :
Packaging : 7
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Dosage Form :
Brand Name : Subutex
Dosage Strength :
Packaging : 7
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
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