01 1ABBVIE
02 2DR REDDYS
03 1ABBOTT
04 2ABRAXIS PHARM
05 2ENDO OPERATIONS
06 4HOSPIRA
07 6IGI LABS INC
08 2QUAD PHARMS
09 4RISING
10 4SOMERSET THERAPS LLC
01 26INJECTABLE;INJECTION
02 2Injectable; Injection
01 18DISCN
02 8RX
03 2Blank
01 4NALBUPHINE
02 22NALBUPHINE HYDROCHLORIDE
03 2NUBAIN
01 24No
02 2Yes
03 2Blank
RLD : No
TE Code :
Brand Name : NALBUPHINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1.5MG/ML
Approval Date : 1993-03-12
Application Number : 20200
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code :
Brand Name : NALBUPHINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/ML
Approval Date : 1998-03-19
Application Number : 74471
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code :
Brand Name : NALBUPHINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/ML
Approval Date : 1998-03-19
Application Number : 74471
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : NALBUPHINE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/ML
Approval Date : 1986-07-02
Application Number : 70751
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : NALBUPHINE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/ML
Approval Date : 1986-09-24
Application Number : 70752
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AP
Brand Name : NALBUPHINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/ML
Approval Date : 1989-02-03
Application Number : 70914
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD :
TE Code :
Brand Name : NALBUPHINE
Dosage Form : Injectable; Injection
Dosage Strength : 10MG/ML
Approval Date :
Application Number : 70692
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Brand Name : NALBUPHINE
Dosage Form : Injectable; Injection
Dosage Strength : 20MG/ML
Approval Date :
Application Number : 70693
RX/OTC/DISCN :
RLD :
TE Code :
Brand Name : NUBAIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 18024
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Brand Name : NUBAIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-05-27
Application Number : 18024
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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