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ACETAMINOPHEN AND CODEINE PHOSPHATE

Approved
Approval ID

17b567bb-05c1-4309-b8ea-59009f08abd5

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 16, 2010

Manufacturers
FDA

Contract Pharmacy Services-PA

DUNS: 945429777

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 Code67046-901
Application NumberANDA040419
Product Classification
M
Marketing Category
C73584
G
Generic Name
acetaminophen and codeine phosphate
Product Specifications
Route of AdministrationORAL
Effective DateOctober 12, 2009
FDA Product Classification

INGREDIENTS (8)

ACETAMINOPHENActive
Quantity: 300 mg in 1 1
Code: 362O9ITL9D
Classification: ACTIB
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
POVIDONEInactive
Code: FZ989GH94E
Classification: IACT
CODEINE PHOSPHATEActive
Quantity: 30 mg in 1 1
Code: GSL05Y1MN6
Classification: ACTIB
CROSPOVIDONEInactive
Code: 68401960MK
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT

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ACETAMINOPHEN AND CODEINE PHOSPHATE - FDA Drug Approval Details