Acetaminophen and Codeine Phosphate
Approved
Approval ID
2f92c67b-f324-4c4e-89fd-1e0f8af96fba
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 31, 2010
Manufacturers
FDA
Rebel Distributors Corp.
DUNS: 118802834
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Acetaminophen and Codeine Phosphate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-547
Application NumberANDA087508
Product Classification
M
Marketing Category
C73584
G
Generic Name
Acetaminophen and Codeine Phosphate
Product Specifications
Route of AdministrationORAL
Effective DateOctober 27, 2006
FDA Product Classification
INGREDIENTS (10)
AlcoholInactive
Code: 3K9958V90M
Classification: IACT
SACCHARIN SODIUMInactive
Code: SB8ZUX40TY
Classification: IACT
SucroseInactive
Code: C151H8M554
Classification: IACT
Codeine PhosphateActive
Quantity: 12 mg in 5 mL
Code: GSL05Y1MN6
Classification: ACTIB
Propylene GlycolInactive
Code: 6DC9Q167V3
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
AcetaminophenActive
Quantity: 120 mg in 5 mL
Code: 362O9ITL9D
Classification: ACTIB
GlycerinInactive
Code: PDC6A3C0OX
Classification: IACT
FD&C RED NO. 40Inactive
Code: WZB9127XOA
Classification: IACT
FD&C YELLOW NO. 6Inactive
Code: H77VEI93A8
Classification: IACT