Label: CHLORZOXAZONE tablet
- NDC Code(s): 68462-724-01, 68462-724-05, 68462-725-01, 68462-725-05
- Packager: Glenmark Pharmaceuticals Inc., USA
- Category: HUMAN PRESCRIPTION DRUG LABEL
Updated April 5, 2021
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Each 375 mg Chlorzoxazone Tablet USP contains: chlorzoxazone USP, 375 mg.
Each 750 mg Chlorzoxazone Tablet USP contains: chlorzoxazone USP, 750 mg.
Chemical Name: 5-Chloro-2-benzoxazolinone.
Molecular Formula: C7H4ClNO2
Molecular Weight: 169.56 g/mol
Chlorzoxazone USP is a white or practically white, practically odorless, crystalline powder.
Chlorzoxazone USP is slightly soluble in water; sparingly soluble in alcohol, in isopropyl alcohol, and in methanol; soluble in solutions of alkali hydroxides and ammonia.
Inactive ingredients: anhydrous lactose, colloidal silicon dioxide, croscarmellose sodium, docusate sodium, magnesium stearate, microcrystalline cellulose, pregelatinized starch and sodium benzoate.
Chlorzoxazone is a centrally-acting agent for painful musculoskeletal conditions. Data available from animal experiments as well as human study indicate that chlorzoxazone acts primarily at the level of the spinal cord and subcortical areas of the brain where it inhibits multisynaptic reflex arcs involved in producing and maintaining skeletal muscle spasm of varied etiology. The clinical result is a reduction of the skeletal muscle spasm with relief of pain and increased mobility of the involved muscles. Blood levels of chlorzoxazone can be detected in people during the first 30 minutes and peak levels may be reached, in the majority of the subjects, in about 1 to 2 hours after oral administration of chlorzoxazone. Chlorzoxazone is rapidly metabolized and is excreted in the urine, primarily in a conjugated form as the glucuronide. Less than one percent of a dose of chlorzoxazone is excreted unchanged in the urine in 24 hours.
INDICATIONS AND USAGE
Chlorzoxazone tablets are indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions. The mode of action of this drug has not been clearly identified, but may be related to its sedative properties. Chlorzoxazone does not directly relax tense skeletal muscles in man.
Serious (including fatal) hepatocellular toxicity has been reported rarely in patients receiving chlorzoxazone. The mechanism is unknown but appears to be idiosyncratic and unpredictable. Factors predisposing patients to this rare event are not known. Patients should be instructed to report early signs and/or symptoms of hepatoxicity such as fever, rash, anorexia, nausea, vomiting, fatigue, right upper quadrant pain, dark urine, or jaundice. Chlorzoxazone tablets should be discontinued immediately and a physician consulted if any of these signs or symptoms develop. Chlorzoxazone tablets use should also be discontinued if a patient develops abnormal liver enzymes (e.g., AST, ALT, alkaline phosphatase and bilirubin).
The concomitant use of alcohol or other central nervous system depressants may have an additive effect.
Usage in Pregnancy: The safe use of chlorzoxazone has not been established with respect to the possible adverse effects upon fetal development. Therefore, it should be used in women of childbearing potential only when, in the judgement of the physician, the potential benefits outweigh the possible risks.
Chlorzoxazone tablets should be used with caution in patients with known allergies or with a history of allergic reactions to drugs. If sensitivity reaction occurs such as urticaria, redness, or itching of the skin, the drug should be stopped.
If any symptoms suggestive of liver dysfunction are observed, the drug should be discontinued.
Chlorzoxazone-containing products are usually well tolerated. It is possible in rare instances that chlorzoxazone may have been associated with gastrointestinal bleeding. Drowsiness, dizziness, light-headedness, malaise, or overstimulation may be noted by an occasional patient. Rarely, allergic-type skin rashes, petechiae, or ecchymoses may develop during treatment. Angioneurotic edema or anaphylactic reactions are extremely rare. There is no evidence that the drug will cause renal damage. Rarely, a patient may note discoloration of the urine resulting from a phenolic metabolite of chlorzoxazone. This finding is of no known clinical significance.
Symptoms: Initially, gastrointestinal disturbances such as nausea, vomiting, or diarrhea together with drowsiness, dizziness, lightheadedness or headache may occur. Early in the course there may be malaise or sluggishness followed by marked loss of muscle tone, making voluntary movement impossible. The deep tendon reflexes may be decreased or absent. The sensorium remains intact, and there is no peripheral loss of sensation. Respiratory depression may occur with rapid, irregular respiration and intercostals and substernal retraction. The blood pressure is lowered, but shock has not been observed.
Treatment: Gastric lavage or induction of emesis should be carried out, followed by administration of activated charcoal. Thereafter, treatment is entirely supportive. If respirations are depressed, oxygen and artificial respiration should be employed and a patent airway assured by use of an oropharyngeal airway or endotracheal tube. Hypotension may be counteracted by use of dextran, plasma, concentrated albumin or a vasopressor agent such as norepinephrine. Cholinergic drugs or analeptic drugs are of no value and should not be used.
DOSAGE AND ADMINISTRATION
Usual Adult Dosage
Chlorzoxazone Tablets USP, 375 mg:
One tablet, three or four times daily. If adequate response is not obtained with this dose, the 375 mg tablets may be increased to two tablets (750 mg) three or four times daily. As improvement occurs, dosage can usually be reduced.
Chlorzoxazone Tablets USP, 750 mg:
1/3 tablet (250 mg) three or four times daily. Initial dosage for painful musculoskeletal conditions should be 2/3 tablet (500 mg) three or four times daily. If adequate response is not obtained with this dose, it may be increased to one tablet (750 mg) three or four times daily. As improvement occurs dosage can usually be reduced.
Chlorzoxazone Tablets USP are supplied as follows:
A white to off-white capsule shaped tablet, debossed with “G” on one side and “724” on the other side, in bottles of 100 and 500 tablets.
- 100’s HDPE bottle pack NDC 68462-724-01
- 500’s HDPE bottle pack NDC 68462-724-05
A white to off-white capsule shaped tablet, debossed with “G” and “725” on the bisected scored side and plain on the trisected scored side, in bottles of 100 and 500 tablets.
- 100’s HDPE bottle pack NDC 68462-725-01
- 500’s HDPE bottle pack NDC 68462-725-05
Dispense in a tight container as defined in the official compendium.
Store at 20°C to 25°C (68°F to 77°F) [see USP Controlled Room Temperature].
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INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68462-724 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORZOXAZONE (UNII: H0DE420U8G) (CHLORZOXAZONE - UNII:H0DE420U8G) CHLORZOXAZONE 375 mg Inactive Ingredients Ingredient Name Strength ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) DOCUSATE SODIUM (UNII: F05Q2T2JA0) MAGNESIUM STEARATE (UNII: 70097M6I30) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM BENZOATE (UNII: OJ245FE5EU) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color WHITE Score no score Shape CAPSULE (CAPSULE-SHAPED) Size 16mm Flavor Imprint Code G;724 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68462-724-01 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/26/2020 2 NDC:68462-724-05 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA212185 05/26/2020 CHLORZOXAZONE
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68462-725 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORZOXAZONE (UNII: H0DE420U8G) (CHLORZOXAZONE - UNII:H0DE420U8G) CHLORZOXAZONE 750 mg Inactive Ingredients Ingredient Name Strength ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) DOCUSATE SODIUM (UNII: F05Q2T2JA0) MAGNESIUM STEARATE (UNII: 70097M6I30) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM BENZOATE (UNII: OJ245FE5EU) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color WHITE Score 3 pieces Shape CAPSULE (CAPSULE-SHAPED) Size 20mm Flavor Imprint Code G;725 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68462-725-01 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/26/2020 2 NDC:68462-725-05 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA212185 05/26/2020 Labeler - Glenmark Pharmaceuticals Inc., USA (130597813) Establishment Name Address ID/FEI Business Operations Glenmark Pharmaceuticals Inc., USA 079922908 MANUFACTURE(68462-724, 68462-725) , ANALYSIS(68462-724, 68462-725)