Hydrocodone Bitartrate and Acetaminophen

Product NDC

63739-326

11-digit product format

637390326

Labeler code

63739

Product ID

63739-326_3cc564c7-5ba5-424d-9dfe-60e47d759e9d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrocodone Bitartrate and Acetaminophen

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation

Application

ANDA040736

Marketing category

ANDA

Marketing start

2010-01-18

Marketing end

0000-00-00

Substance

HYDROCODONE BITARTRATE; ACETAMINOPHEN

Active strength

5 mg/1; mg/1

Pharmacologic classes

Opioid Agonist [EPC],Opioid Agonists [MoA]

DEA schedule

CII

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record