Label: METHOCARBAMOL tablet
Contains inactivated NDC Code(s)
NDC Code(s): 65977-5033-0, 65977-5033-1, 65977-5033-2, 65977-5033-3, view more65977-5033-4, 65977-5034-0, 65977-5034-1, 65977-5034-2, 65977-5034-3
- Packager: Hetero Drugs Limited Unit III
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Updated December 17, 2009
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Methocarbamol tablets USP a carbamate derivative of guaifenesin, is a central nervous system (CNS) depressant with sedative and musculoskeletal relaxant properties.
The chemical name of methocarbamol is 3-(2-methoxyphenoxy)-1,2-propanediol 1-carbamate and has the empirical formula C11H15NO5. Its molecular weight is 241.24. The structural formula is shown below.
Methocarbamol is a white powder, sparingly soluble in water and chloroform, soluble in alcohol (only with heating) and propylene glycol, and insoluble in benzene and n-hexane.
Methocarbamol tablets USP are available as 500 mg and 750 mg tablets for oral administration. Methocarbamol tablets USP 500 mg and 750 mg contain the following inactive ingredients: sodium lauryl sulfate, sodium starch glycolate, povidone K 90, polyethylene glycol, magnesium stearate, colloidal silicon dioxide, low substituted hydroxy propyl cellulose and stearic acid.
The mechanism of action of methocarbamol in humans has not been established, but may be due to general central nervous system (CNS) depression. It has no direct action on the contractile mechanism of striated muscle, the motor end plate or the nerve fiber.
In healthy volunteers, the plasma clearance of methocarbamol ranges between 0.20 and 0.80 L/h/kg, the mean plasma elimination half-life ranges between 1 and 2 hours, and the plasma protein binding ranges between 46% and 50%.
Methocarbamol is metabolized via dealkylation and hydroxylation. Conjugation of methocarbamol also is likely. Essentially all methocarbamol metabolites are eliminated in the urine. Small amounts of unchanged methocarbamol also are excreted in the urine.
The mean (± SD) elimination half-life of methocarbamol in elderly healthy volunteers
(mean (± SD) age, 69 (± 4) years) was slightly prolonged compared to a younger (mean (± SD) age, 53.3 (± 8.8) years), healthy population (1.5 (± 0.4) hours versus 1.1 (± 0.27) hours, respectively). The fraction of bound methocarbamol was slightly decreased in the elderly versus younger volunteers (41 to 43% versus 46 to 50%, respectively).
The clearance of methocarbamol in 8 renally-impaired patients on maintenance hemodialysis was reduced about 40% compared to 17 normal subjects, although the mean ( ± SD) elimination half-life in these two groups was similar: 1.2 ( ± 0.6) versus 1.1 ( ± 0.3) hours, respectively
In 8 patients with cirrhosis secondary to alcohol abuse, the mean total clearance of methocarbamol was reduced approximately 70% compared to that obtained in 8 age- and weight-matched normal subjects.The mean ( ± SD) elimination half-life in the cirrhotic patients and the normal subjects was 3.38 ( ± 1.62) hours and 1.11 ( ± 0.27) hours, respectively. The percent of methocarbamol bound to plasma proteins was decreased to approximately 40 to 45% compared to 46 to 50% in the normal subjects.
INDICATIONS AND USAGE
Methocarbamol tablets USP 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 methocarbamol has not been clearly identified, but may be related to its sedative properties. Methocarbamol does not directly relax tense skeletal muscles in man.
Since methocarbamol may possess a general CNS depressant effect, patients receiving methocarbamol tablets USP should be cautioned about combined effects with alcohol and other CNS depressants.
Safe use of methocarbamol tablets USP has not been established with regard to possible adverse effects upon fetal development. There have been reports of fetal and congenital abnormalities following in utero exposure to methocarbamol. Therefore, methocarbamol tablets USP should not be used in women who are or may become pregnant and particularly during early pregnancy unless in the judgment of the physician the potential benefits outweigh the possible hazards (see PRECAUTIONS, Pregnancy)
Use In Activities Requiring Mental Alertness
Methocarbamol may impair mental and/or physical abilities required for performance of hazardous tasks, such as operating machinery or driving a motor vehicle. Patients should be cautioned about operating machinery, including automobiles, until they are reasonably certain that methocarbamol therapy does not adversely affect their ability to engage in such activities.
Information for Patients
Patients should be cautioned that methocarbamol may cause drowsiness or dizziness, which may impair their ability to operate motor vehicles or machinery.
Because methocarbamol may possess a general CNS-depressant effect, patients should be cautioned about combined effects with alcohol and other CNS depressants.
Methocarbamol may inhibit the effect of pyridostigmine bromide. Therefore, methocarbamol should be used with caution in patients with myasthenia gravis receiving anticholinesterase agents
Drug or Laboratory Test Interactions
Methocarbamol may cause a color interference in certain screening tests for 5-hydroxyindoleacetic acid (5-HIAA) using nitrosonaphthol reagent and in screening tests for urinary vanillylmandelic acid (VMA) using the Gitlow method.
Carcinogenesis,Mutagenesis,Impairment of Fertility
Long-term studies to evaluate the carcinogenic potential of methocarbamol have not been performed. No studies have been conducted to assess the effect of methocarbamol on mutagenesis or its potential to impair fertility.
Teratogenic effects -Pregnancy Category C
Animal reproduction studies have not been conducted with methocarbamol. It is also not known whether methocarbamol can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Methocarbamol tablets USP should be given to a pregnant woman only if clearly needed.
Safe use of methocarbamol tablets USP has not been established with regard to possible adverse effects upon fetal development. There have been reports of fetal and congenital abnormalities following in utero exposure to methocarbamol. Therefore, methocarbamol tablets USP should not be used in women who are or may become pregnant and particularly during early pregnancy unless in the judgment of the physician the potential benefits outweigh the possible hazards (seeWARNINGS ).
Methocarbamol and/or its metabolites are excreted in the milk of dogs; however, it is not known whether methocarbamol or its metabolites are excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when methocarbamol tablets USP are administered to a nursing woman
Adverse reactions reported coincident with the administration of methocarbamol include:
Body as a whole: Anaphylactic reaction, angioneurotic edema, fever, headache
Cardiovascular system: Bradycardia, flushing, hypotension, syncope, thrombophlebitis
Digestive system: Dyspepsia, jaundice (including cholestatic jaundice), nausea and vomiting
Hemic and lymphatic system: Leukopenia
Immune system: Hypersensitivity reactions
Nervous system: Amnesia, confusion, diplopia, dizziness or lightheadedness, drowsiness, insomnia, mild muscular incoordination, nystagmus, sedation, seizures (including grand mal), vertigo
Skin and special senses: Blurred vision, conjunctivitis, nasal congestion, metallic taste, pruritus, rash, urticaria
Limited information is available on the acute toxicity of methocarbamol. Overdose of methocarbamol is frequently in conjunction with alcohol or other CNS depressants and includes the following symptoms: nausea, drowsiness, blurred vision, hypotension, seizures, and coma.
In post-marketing experience, deaths have been reported with an overdose of methocarbamol alone or in the presence of other CNS depressants, alcohol or psychotropic drugs.
Management of overdose includes symptomatic and supportive treatment. Supportive measures include maintenance of an adequate airway, monitoring urinary output and vital signs, and administration of intravenous fluids if necessary. The usefulness of hemodialysis in managing overdose is unknown
DOSAGE & ADMINISTRATION
Methocarbamol Tablets USP 500 mg – Adults:
Initial dosage: 3 tablets q.i.d.
Maintenance dosage: 2 tablets q.i.d.
Methocarbamol Tablets USP 750 mg – Adults:
Initial dosage: 2 tablets q.i.d.
Maintenance dosage: 1 tablet q.4h. or 2 tablets t.i.d.
Six grams a day are recommended for the first 48 to 72 hours of treatment. (For severe conditions 8 grams a day may be administered). Thereafter, the dosage can usually be reduced to approximately 4 grams a day.
Methocarbamol tablets USP 500 mg are white to off white, capsule shaped, tablets debossed with ‘H’ on scored side and ‘114’ on unscored side . They are supplied as follows:
Bottles of 30 NDC 65977-5033-0
Bottles of 60 NDC 65977-5033-1
Bottles of 100 NDC 65977-5033-2
Bottles of 500 NDC 65977-5033-3
Bottles of 1000 NDC 65977-5033-4
Methocarbamol tablets USP 750 mg are white to off white, capsule shaped, tablets debossed with ‘H’ on one side and ‘115’ on other side . They are supplied as follows:
Bottles of 30 NDC 65977-5034-0
Bottles of 60 NDC 65977-5034-1
Bottles of 100 NDC 65977-5034-2
Bottles of 500 NDC 65977-5034-3
Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
Dispense in tight container.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Methocarbamol tablets, USP 500 mg 30 tablets
Methocarbamol tablets, USP 500 mg 60 tablets
Methocarbamol tablets, USP 500 mg 100 tablets
Methocarbamol tablets, USP 500 mg 500 tablets
Methocarbamol tablets, USP 500 mg 1000 tablets
Methocarbamol tablets, USP 750 mg 30 tablets
Methocarbamol tablets, USP 750 mg 60 tablets
Methocarbamol tablets, USP 750 mg 100 tablets
Methocarbamol tablets, USP 750 mg 500 tablets
INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65977-5033 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Methocarbamol (UNII: 125OD7737X) (Methocarbamol - UNII:125OD7737X) Methocarbamol 500 mg Inactive Ingredients Ingredient Name Strength sodium lauryl sulfate (UNII: 368GB5141J) Sodium Starch Glycolate Type A Potato (UNII: 5856J3G2A2) Povidone K90 (UNII: RDH86HJV5Z) polyethylene glycol (UNII: 3WJQ0SDW1A) magnesium stearate (UNII: 70097M6I30) colloidal silicon dioxide (UNII: ETJ7Z6XBU4) Hydroxypropyl Cellulose, Low Substituted (UNII: 2165RE0K14) stearic acid (UNII: 4ELV7Z65AP) Product Characteristics Color WHITE (White to off White) Score 2 pieces Shape CAPSULE (capsule) Size 14mm Flavor Imprint Code H;114 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65977-5033-0 30 in 1 BOTTLE 2 NDC:65977-5033-1 60 in 1 BOTTLE 3 NDC:65977-5033-2 100 in 1 BOTTLE 4 NDC:65977-5033-3 500 in 1 BOTTLE 5 NDC:65977-5033-4 1000 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA090200 11/06/2009 METHOCARBAMOL
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65977-5034 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Methocarbamol (UNII: 125OD7737X) (Methocarbamol - UNII:125OD7737X) Methocarbamol 750 mg Inactive Ingredients Ingredient Name Strength sodium lauryl sulfate (UNII: 368GB5141J) Sodium Starch Glycolate Type A Potato (UNII: 5856J3G2A2) povidone K90 (UNII: RDH86HJV5Z) polyethylene glycol (UNII: 3WJQ0SDW1A) magnesium stearate (UNII: 70097M6I30) colloidal silicon dioxide (UNII: ETJ7Z6XBU4) Hydroxypropyl Cellulose, Low Substituted (UNII: 2165RE0K14) stearic acid (UNII: 4ELV7Z65AP) Product Characteristics Color WHITE (White to off White) Score no score Shape CAPSULE (capsule) Size 19mm Flavor Imprint Code H;115 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65977-5034-0 30 in 1 BOTTLE 2 NDC:65977-5034-1 60 in 1 BOTTLE 3 NDC:65977-5034-2 100 in 1 BOTTLE 4 NDC:65977-5034-3 500 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA090200 11/06/2009 Labeler - Hetero Drugs Limited Unit III (650220163) Establishment Name Address ID/FEI Business Operations Hetero Drugs Limited Unit III 650220163 analysis, manufacture