Please Wait
Applying Filters...
Menu
Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 2ORGANON USA INC

02 2QUAD PHARMS

03 2WATSON LABS

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

NANDROLONE PHENPROPIONATE

Brand Name : NANDROLONE PHENPROPIONATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 25MG/ML

Approval Date : 1983-06-17

Application Number : 86386

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

02

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

NANDROLONE PHENPROPIONATE

Brand Name : NANDROLONE PHENPROPIONATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML

Approval Date : 1983-06-17

Application Number : 87488

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

03

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

NANDROLONE PHENPROPIONATE

Brand Name : DURABOLIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 25MG/ML

Approval Date : 1982-01-01

Application Number : 11891

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

04

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

NANDROLONE PHENPROPIONATE

Brand Name : DURABOLIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML

Approval Date : 1982-01-01

Application Number : 11891

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

05

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

NANDROLONE PHENPROPIONATE

Brand Name : NANDROLONE PHENPROPIONATE

Dosage Form : Injectable; Injection

Dosage Strength : 25MG/ML

Approval Date :

Application Number : 89297

RX/OTC/DISCN :

RLD :

TE Code :

blank

06

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

NANDROLONE PHENPROPIONATE

Brand Name : NANDROLONE PHENPROPIONATE

Dosage Form : Injectable; Injection

Dosage Strength : 50MG/ML

Approval Date :

Application Number : 89298

RX/OTC/DISCN :

RLD :

TE Code :

blank