LIDOCAINE- lidocaine patch

Country: Stati Uniti

Lingwa: Ingliż

Sors: NLM (National Library of Medicine)

Ixtrih issa

Ingredjent attiv:

LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)

Disponibbli minn:

Preferred Pharmaceuticals Inc.

INN (Isem Internazzjonali):

LIDOCAINE

Kompożizzjoni:

LIDOCAINE 700 mg

Rotta amministrattiva:

CUTANEOUS

Tip ta 'preskrizzjoni:

PRESCRIPTION DRUG

Indikazzjonijiet terapewtiċi:

Lidocaine patch 5% is contraindicated in patients with a known history of sensitivity to local anesthetics of the amide type, or to any other component of the product.

Sommarju tal-prodott:

Lidocaine patch 5% is available as the following: Carton of 30 patches, packaged into individual child-resistant envelopes. NDC 68788-6433-3 Store at 20o to 25o C (68o to 77o F) [See USP Controlled Room Temperature]. For more information, call Actavis at 1-800-272-5525. Manufactured by: Actavis Laboratories UT, Inc. Salt Lake City, UT 84108 USA Distributed by:            Actavis Pharma, Inc. Parsippany, NJ 07054 USA Revised: February 2015 Relabeled By: Preferred Pharmaceuticals Inc .

L-istatus ta 'awtorizzazzjoni:

Abbreviated New Drug Application

Karatteristiċi tal-prodott

                                LIDOCAINE- LIDOCAINE PATCH
PREFERRED PHARMACEUTICALS INC.
----------
LIDOCAINE PATCH
LIDOCAINE PATCH 5%
Revised: February 2015
RX ONLY
DESCRIPTION
Lidocaine patch 5% is comprised of an adhesive material containing 5%
lidocaine, which is applied to a
white non-woven polyethylene terephthalate (PET) material backing and
covered with a transparent PET
release liner. The release liner is removed prior to application to
the skin. The size of the patch is 10
cm x 14 cm.
Lidocaine is chemically designated as acetamide,
2-(diethylamino)-N-(2,6-dimethylphenyl), has an
octanol:water partition ratio of 43 at pH 7.4, and has the following
structure:
Each adhesive patch contains 700 mg of lidocaine (50 mg per gram
adhesive) in an aqueous base. It also
contains the following inactive ingredients: glycerin, D-sorbitol,
propylene glycol, polyvinyl alcohol,
urea, sodium polyacrylate, carboxymethylcellulose sodium, gelatin,
polyacrylic acid, kaolin, tartaric
acid, dihydroxyaluminum aminoacetate, methylparaben, propylparaben,
and edetate disodium.
CLINICAL PHARMACOLOGY
_PHARMACODYNAMICS_
Lidocaine is an amide-type local anesthetic agent and is suggested to
stabilize neuronal membranes by
inhibiting the ionic fluxes required for the initiation and conduction
of impulses.
The penetration of lidocaine into intact skin after application of
lidocaine patch is sufficient to produce
an analgesic effect, but less than the amount necessary to produce a
complete sensory block.
_PHARMACOKINETICS_
_ABSORPTION:_
The amount of lidocaine systemically absorbed from lidocaine patch is
directly related to both the
duration of application and the surface area over which it is applied.
In a pharmacokinetic study, three
lidocaine patches were applied over an area of 420 cm of intact skin
on the back of normal volunteers
for 12 hours. Blood samples were withdrawn for determination of
lidocaine concentration during the
application and for 12 hours after removal of patches. The results are
summarized in Table 1.
TABLE 1 ABSORPTION OF LIDOCAINE FROM LIDOCA
                                
                                Aqra d-dokument sħiħ
                                
                            

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