nalbuphine

North America

Canada (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
NUBAIN INJECTION 10MG/ML sol
Schedule G (CDSA IV)
iv/im/subcut
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
NUBAIN INJECTION 10MG/ML sol
01913980
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United States (15)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
NALBUPHINE 10MG/ML inj
N
INJECTION
N02AF02
NALBUPHINE 10MG/ML inj
N
Injection
N02AF02
NALBUPHINE 20MG/ML inj
N
INJECTION
N02AF02
NALBUPHINE 20MG/ML inj
N
Injection
N02AF02
NALBUPHINE HYDROCHLORIDE 1.5MG/ML inj
N
INJECTION
N02AF02
NALBUPHINE HYDROCHLORIDE 10MG/ML inj
N
INJECTION
N02AF02
NALBUPHINE HYDROCHLORIDE 10MG/ML inj
Y
Y
Rx
Rx
INJECTION
N02AF02
NALBUPHINE HYDROCHLORIDE 10MG/ML inj
N
N
N


INJECTION
N02AF02
NALBUPHINE HYDROCHLORIDE 10MG/ML inj
N
N

INJECTION
N02AF02
NALBUPHINE HYDROCHLORIDE 20MG/ML inj
N
INJECTION
N02AF02
NALBUPHINE HYDROCHLORIDE 20MG/ML inj
N
INJECTION
N02AF02
NALBUPHINE HYDROCHLORIDE 20MG/ML inj
Y
Y
Rx
Rx
INJECTION
N02AF02
NALBUPHINE HYDROCHLORIDE 20MG/ML inj
N
N
N


INJECTION
N02AF02
NALBUPHINE HYDROCHLORIDE 20MG/ML inj
N
N

INJECTION
N02AF02
NUBAIN inj
N
N

INJECTION
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
NALBUPHINE 10MG/ML inj
70751/1
ANDA
02-07-1986
NALBUPHINE 10MG/ML inj
70692/1
ANDA
NALBUPHINE 20MG/ML inj
70752/1
ANDA
24-09-1986
NALBUPHINE 20MG/ML inj
70693/1
ANDA
NALBUPHINE HYDROCHLORIDE 1.5MG/ML inj
20200/1
NDA
12-03-1993
NALBUPHINE HYDROCHLORIDE 10MG/ML inj
74471/1
ANDA
19-03-1998
NALBUPHINE HYDROCHLORIDE 10MG/ML inj
70915/1
70914/1
ANDA
ANDA
03-02-1989
03-02-1989
NALBUPHINE HYDROCHLORIDE 10MG/ML inj
72072/1
72071/1
72070/1
ANDA
ANDA
ANDA
10-04-1989
10-04-1989
10-04-1989
NALBUPHINE HYDROCHLORIDE 10MG/ML inj
207595/1
206506/1
ANDA
ANDA
11-01-2019
06-02-2019
NALBUPHINE HYDROCHLORIDE 20MG/ML inj
70917/1
ANDA
03-02-1989
NALBUPHINE HYDROCHLORIDE 20MG/ML inj
74471/2
ANDA
19-03-1998
NALBUPHINE HYDROCHLORIDE 20MG/ML inj
70918/1
70916/1
ANDA
ANDA
03-02-1989
03-02-1989
NALBUPHINE HYDROCHLORIDE 20MG/ML inj
72073/1
72075/1
72074/1
ANDA
ANDA
ANDA
10-04-1989
10-04-1989
10-04-1989
NALBUPHINE HYDROCHLORIDE 20MG/ML inj
207595/2
206506/2
ANDA
ANDA
11-01-2019
06-02-2019
NUBAIN inj
18024/1
18024/2
NDA
NDA
01-01-1982
27-05-1982
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Europe

Austria (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
NALBUPHIN AMOMED 10 MG/ML sol for inj
Rx
-
N02AF02
NUBAIN 10 MG/ML sol for inj
Rx
-
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
NALBUPHIN AMOMED 10 MG/ML sol for inj
1-26798
20-12-2006
NUBAIN 10 MG/ML sol for inj
140200
09-07-2020
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.

Belgium (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PAINAFIN 10 MG/ML sol for inj
2 mL
-
iv/im/subcut
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PAINAFIN 10 MG/ML sol for inj
2 mL
BE404485
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
PAINAFIN 10 MG/ML sol for inj
2 mL
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Bosnia and Herzegovina (0)
No result.
Croatia (0)
No result.
Czechia (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
NALBUPHIN ORPHA 10MG/ML sol for inj
10MG/ML 10X2ML
Y
iv/im/subcut
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
NALBUPHIN ORPHA 10MG/ML sol for inj
10MG/ML 10X2ML
65/ 622/07-C
MRP/DCP
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
NALBUPHIN ORPHA 10MG/ML sol for inj
10MG/ML 10X2ML
591,25
838,75
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Denmark (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
NALPAIN 10 MG/ML sol for inj
-
-
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
NALPAIN 10 MG/ML sol for inj
28104063207
MRP
19-07-2007
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
NALPAIN 10 MG/ML sol for inj
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.

Finland (0)
No result.
Hungary (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
BUFIMORF 10 MG/ML sol for inj
10x2ml amp
N
Rx
parenteral
N02AF02
NALPAIN 10 MG/ML sol for inj
10x amp
Y
Rx
-
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
BUFIMORF 10 MG/ML sol for inj
10x2ml amp
OGYI-T-20003/01
21-12-2005
NALPAIN 10 MG/ML sol for inj
10x amp
OGYI-T-22407/01
23-01-2013
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
BUFIMORF 10 MG/ML sol for inj
10x2ml amp
0
0
0
0
NALPAIN 10 MG/ML sol for inj
10x amp
0
0
0
0
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Iceland (0)
No result.
Ireland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
LAPAINOL 10 MG/ML sol for inj
N
Rx
iv
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
LAPAINOL 10 MG/ML sol for inj
PA1353/002/001
03-08-2007
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.

Lithuania (0)
No result.
Malta (0)
No result.
Netherlands (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
NALBUFINE HCL ORPHA 10 MG/ML sol for inj
-
Rx
parenteral
N02AF02
NUBAIN 10 MG/ML sol for inj
-
Rx
iv
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
NALBUFINE HCL ORPHA 10 MG/ML sol for inj
RVG 30852
-
23-03-2006
NUBAIN 10 MG/ML sol for inj
RVG 124338
-
22-06-2020
Product
Pack
SPC
PIL
Company
NALBUFINE HCL ORPHA 10 MG/ML sol for inj
NUBAIN 10 MG/ML sol for inj
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.

Norway (0)
No result.
Poland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
NALPAIN 10 MG/ML 10 MG/ML sol for inj
10 amp 2 ml
-
Rx
-
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
NALPAIN 10 MG/ML 10 MG/ML sol for inj
10 amp 2 ml
14424
MRP
Product
Pack
SPC
PIL
Company
NALPAIN 10 MG/ML 10 MG/ML sol for inj
10 amp 2 ml
Would you like to in or out-license dossiers? Do you have Marketing Authorization to sell? Would you like to sell or aquire companies? This is the right place for you to find new business opportunities in the pharmaceutical industry.

Romania (0)
No result.
Slovenia (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
NALPAIN 10 MG/ML sol for inj
10 amp 2 ml sol
N
Rx
iv/im/subcut
N02AF02
NUBAIN sol for inj
10 amp 2 ml sol (20 mg/2 ml)
-
Rx
parenteral
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
NALPAIN 10 MG/ML sol for inj
10 amp 2 ml sol
1013-175/2018-5
MRP
24-03-2021
NUBAIN sol for inj
10 amp 2 ml sol (20 mg/2 ml)
-
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
NALPAIN 10 MG/ML sol for inj
10 amp 2 ml sol
19,96
NUBAIN sol for inj
10 amp 2 ml sol (20 mg/2 ml)
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Spain (0)
No result.
Sweden (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
NALPAIN (FD NALBUFIN ORPHA-DEVEL) 10 MG/ML sol for inj
Rx
-
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
NALPAIN (FD NALBUFIN ORPHA-DEVEL) 10 MG/ML sol for inj
Nationell decentral eller ömsesidig
20-12-2007
25-02-2019
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Switzerland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
NALBUPHIN ORPHA sol for inj
-
A
-
N02AF02
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
NALBUPHIN ORPHA sol for inj
56989 1
Hauptzulassung
15-10-2004
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