MedPath
FDA Approval

Methadone Hydrochloride

September 14, 2022

HUMAN PRESCRIPTION DRUG LABEL

Methadone(10 mg in 1 mL)

Manufacturing Establishments (1)

ATLANTIC BIOLOGICALS CORP.

ATLANTIC BIOLOGICALS CORP.

047437707

Products (1)

Methadone Hydrochloride

17856-0392

ANDA040180

ANDA (C73584)

ORAL

September 14, 2022

ANHYDROUS CITRIC ACIDInactive
Code: XF417D3PSLClass: IACT
D&C RED NO. 33Inactive
Code: 9DBA0SBB0LClass: IACT
GLYCERINInactive
Code: PDC6A3C0OXClass: IACT
SORBITOLInactive
Code: 506T60A25RClass: IACT
SODIUM BENZOATEInactive
Code: OJ245FE5EUClass: IACT
SUCROSEInactive
Code: C151H8M554Class: IACT
WATERInactive
Code: 059QF0KO0RClass: IACT
CHERRYInactive
Code: BUC5I9595WClass: IACT
SACCHARIN SODIUMInactive
Code: SB8ZUX40TYClass: IACT
MethadoneActive
Code: 229809935BClass: ACTIBQuantity: 10 mg in 1 mL
FD&C RED NO. 40Inactive
Code: WZB9127XOAClass: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3Class: IACT
© Copyright 2025. All Rights Reserved by MedPath