01 1ABBVIE
02 2DR REDDYS
03 1ABBOTT
04 4ABRAXIS PHARM
05 4HOSPIRA
06 8IGI LABS INC
07 5PH HEALTH
08 2QUAD PHARMS
09 4RISING
10 4SOMERSET THERAPS LLC
01 1INJECTABLE;INJECTION
02 2Injectable; Injection
03 32SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
01 25DISCN
02 8RX
03 2Blank
01 5NALBUPHINE
02 25NALBUPHINE HYDROCHLORIDE
03 5NUBAIN
01 28No
02 5Yes
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 : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 100MG/10ML (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 : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 200MG/10ML (20MG/ML)
Approval Date : 1998-03-19
Application Number : 74471
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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 :
RLD : Yes
TE Code :
Brand Name : NUBAIN
Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 10MG/ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
RLD : Yes
TE Code :
Brand Name : NUBAIN
Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 20MG/ML (20MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
RLD : Yes
TE Code :
Brand Name : NUBAIN
Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 100MG/10ML (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
RLD : Yes
TE Code :
Brand Name : NUBAIN
Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 20MG/2ML (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
RLD : Yes
TE Code :
Brand Name : NUBAIN
Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 200MG/10ML (20MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1984-03-02
Application Number : 18024
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
