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HYDROCODONE BITARTRATE AND ACETAMINOPHEN

CIII Rx only

Approved
Approval ID

a46da71a-5fe1-4021-b866-4a806a12efa8

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 30, 2012

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.

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code42254-340
Application NumberANDA090118
Product Classification
M
Marketing Category
C73584
G
Generic Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Product Specifications
Route of AdministrationORAL
Effective DateJuly 26, 2011
FDA Product Classification

INGREDIENTS (9)

HYDROCODONE BITARTRATEActive
Quantity: 5 mg in 1 1
Code: NO70W886KK
Classification: ACTIB
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
ACETAMINOPHENActive
Quantity: 325 mg in 1 1
Code: 362O9ITL9D
Classification: ACTIB
POVIDONESInactive
Code: FZ989GH94E
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
CROSPOVIDONEInactive
Code: 68401960MK
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT

Drug Labeling Information

Boxed Warning section

LOINC: 34066-1Updated: 5/23/2011

Hepatotoxicity

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HYDROCODONE BITARTRATE AND ACETAMINOPHEN - FDA Drug Approval Details