01 1BRECKENRIDGE
02 2ASCENT PHARMS INC
03 2AUROLIFE PHARMA LLC
04 2ELITE LABS INC
05 2EPIC PHARMA LLC
06 10HIKMA
07 2LANNETT CO INC
08 1LONG GROVE PHARMS
09 3MALLINCKRODT INC
10 1MYLAN INSTITUTIONAL
11 1ROXANE
12 4SANDOZ
13 10SPECGX LLC
14 2SUN PHARM INDUSTRIES
15 2THEPHARMANETWORK LLC
16 7VISTAPHARM LLC
01 7CONCENTRATE;ORAL
02 3INJECTABLE;INJECTION
03 3POWDER;FOR RX COMPOUNDING
04 6SOLUTION;ORAL
05 1SYRUP;ORAL
06 1TABLET, DISPERSIBLE;ORAL
07 3TABLET, EFFERVESCENT;ORAL
08 4TABLET, FOR SUSPENSION;ORAL
09 24TABLET;ORAL
01 19DISCN
02 33RX
01 3DOLOPHINE HYDROCHLORIDE
02 40METHADONE HYDROCHLORIDE
03 1METHADONE HYDROCHLORIDE INTENSOL
04 4METHADOSE
05 4WESTADONE
01 45No
02 7Yes
RLD : No
TE Code : AP
Brand Name : METHADONE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/ML
Approval Date : 2024-12-16
Application Number : 218252
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : Yes
TE Code :
Brand Name : DOLOPHINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 6134
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : DOLOPHINE HYDROCHLORIDE
Dosage Form : SYRUP;ORAL
Dosage Strength : 10MG/30ML
Approval Date : 1982-01-01
Application Number : 6134
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : DOLOPHINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 6134
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AA
Brand Name : METHADONE HYDROCHLORIDE
Dosage Form : TABLET, FOR SUSPENSION;ORAL
Dosage Strength : 40MG
Approval Date : 1982-01-01
Application Number : 17058
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AA
RLD : No
TE Code :
Brand Name : METHADONE HYDROCHLORIDE
Dosage Form : POWDER;FOR RX COMPOUNDING
Dosage Strength : 50GM/BOT
Approval Date : 1982-01-01
Application Number : 6383
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : METHADONE HYDROCHLORIDE
Dosage Form : POWDER;FOR RX COMPOUNDING
Dosage Strength : 100GM/BOT
Approval Date : 1982-01-01
Application Number : 6383
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : METHADONE HYDROCHLORIDE
Dosage Form : POWDER;FOR RX COMPOUNDING
Dosage Strength : 500GM/BOT
Approval Date : 1982-01-01
Application Number : 6383
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : WESTADONE
Dosage Form : TABLET, DISPERSIBLE;ORAL
Dosage Strength : 2.5MG
Approval Date : 1982-01-01
Application Number : 17108
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : WESTADONE
Dosage Form : TABLET, EFFERVESCENT;ORAL
Dosage Strength : 5MG
Approval Date : 1982-01-01
Application Number : 17108
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
