Clanza description, usages, side effects, indications, overdosage, supplying and lots more!

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Clanza

United Douglas Pharm., Inc.
United Douglas Pharm., Inc.




FULL PRESCRIBING INFORMATION

DESCRIPTION

White, oblong, film-coated tablet, engraved with "UT" on one side and "CL CR" on the other side.

Uses

INDICATIONS

CLANZA CR is indicated for Rheumatoid arthritis, ankylosing spondylitis, osteoarthritis and periarthritis of scapulohumerous, lumbago, ischiadynia, pain caused by nonaticular rheutism.

Dosage and Administration

Adults: The recommended dose is 200 mg daily, taken as one dose (every 24 hours).  However, the dose and dose frequency of CLANZA CR can be modified under the supervison of physician or pharmacist.

CONTRAINDICATIONS

Patients with allergy to these drugs or other analogues (diclofenac). Patients with asthma. Like NSAIDS, acetylsalicylic acid and other drugs which inhibit prostagladin-synthesis may precipitate attacks of asthma, acute rhinitis or urticaria. Patients with active peptic ulcer.

CAUTIONS

Patients with symptoms indicative of gastro-intestinal disorders, with a history of gastroulceration.  Patients with severe hepatic impairment or cardiac or renal impairment.  Patients under the medication of diuretics.  Patients in recovery after surgical treatment.

ADVERSE REACTIONS

The majority of side effects observed have been reversible and of a minor nature and include gastro-intestinal disorders (dyspepsia, abdominal pain, nausea), rash, ruber, urticaria, symptoms of enuresis, headache, dizziness, and drowsiness.  To report suspected adverse reactions, call 1-800-FDA-1088.

GENERAL PRECAUTIONS

Patients suffering from dizziness, vertigo, or other central nervous system disorders while taking NSAIDS should refrain from driving or handling dangerous machinery.

DRUG INTERACTIONS

There has been no drug interactions reported, but close monitoring of patients on combination with lithium and digoxin, oral antidiabetic agents, anticoagulants, diuretics, and other analgesics.

USE IN PREGNANCY AND NURSING MOTHERS

Since there is no information on the safe use of CLANZA CR during pregnancy and lactation, the use of CLANZA CR should therefore be avoided in pregnancy and lactation.

USE IN CHILDREN

The dosage and indication is not established yet for children with less than 6 years old.

OVERDOSAGE

There are no human data available on the consequences of CLANZA CR overdosage.  If overdosage is observed, therapeutic measures should be taken according to symptoms; supportive and symptomatic treatment should be given for complications such as hypotension, gastro-intestinal irritation, respiratory depression, and convulsions.

STORAGE

Preserve in tight containers.  Store at room temperature not exceeding 30oC.

SHELF LIFE

Three (3) years from manufacturing date.  Do not exceed the expiry date for use printed on the box .

PACKAGE

10 Blister Packs with 10 Tablets in each Blister Pack

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label test Clanza

Clanza

Aceclofenac TABLET, FILM COATED

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:65697-450
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Aceclofenac Aceclofenac 200 mg

Inactive Ingredients

Ingredient Name Strength
lactose monohydrate
cellulose, microcrystalline
SODIUM CARBONATE
COLLOIDAL SILICON DIOXIDE
CROSPOVIDONE
POLOXAMER 407
MAGNESIUM STEARATE
ALCOHOL
HYPROMELLOSE 2208 (15000 MPA.S)
Carbomer 941
HYPROMELLOSE 2910 (6 MPA.S)
ALCOHOL
methylene chloride
Hypromellose 2910 (5 Mpa.s)
titanium dioxide
ETHYLCELLULOSES
diethyl phthalate

Product Characteristics

Color Size Imprint Code Shape
white 15 mm UT;CR;CT OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65697-450-20 1 in 1 PACKET
2 NDC:65697-450-21 10 in 1 BLISTER PACK
3 NDC:65697-450-22 10 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-05-12


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