Identify 2632 V pill’s drug class, dosage, size, shape, side effects, high

2632 V pill's drug class, dosage, size, shape, side effects, high

What is 2632 V pill?

2632 V is an imprint on a pill identified as yellow and round-shaped. The pill contains cyclobenzaprine hydrochloride in the dose of 10 mg. Cyclobenzaprine belongs to the drug class named skeletal muscle relaxants. It is prescribed for the treatment of muscle spasm, fibromyalgia, sciatica, chronic myofascial pain, migraine. It is supplied by Qualitest Pharmaceuticals Inc.

2632 V yellow pill - Street value, uses

  • Imprint: 2632 V
  • Strength: 10 mg
  • Color: Yellow
  • Shape: Round-shape
  • Size: 7 mm
  • Availability: Prescription only
  • Drug Class: Skeletal muscle relaxants
  • Pregnancy Category: B – No proven risk in humans
  • CSA Schedule: Not a controlled drug
  • Labeler / Supplier: Qualitest Pharmaceuticals Inc.
  • National Drug Code (NDC): 00185-0613
  • Inactive Ingredients: croscarmellose sodium, FD&C Yellow No. 6, hypromelloses, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide, D&C Yellow No. 10 and polysorbate 80

2632 V pill other labelers and repackagers

  • 68084-0397 – Amerisource Health Services
  • 63739-0531 – McKesson Packaging Services
  • 43547-0400 – Solco Healthcare U.S., LLC
  • 54569-3193 – A-S Medication Solutions, LLC (repackager)
  • 54569-5184 – A-S Medication Solutions, LLC (repackager)
  • 54569-2573 – A-S Medication Solutions, LLC (repackager)

Active ingredients of 2632 V pill and identification

The only active ingredient in 2632 V pill is cyclobenzaprine. It is is a muscle relaxant that works by blocking nerve impulses or pain sensations that are sent to the brain.

Cyclobenzaprine hydrochloride appears as a white, crystalline tricyclic amine salt. Its melting point is 217°C and a pKa of 8.47 at 25°C. It is freely soluble in water and alcohol and sparingly soluble in isopropanol, and insoluble in hydrocarbon solvents.

2632 V pill chemistry

Cyclobenzaprine:

IUPAC name: 3-(dibenzo[1,2-a:1′,2′-e][7]annulen-11-ylidene)-N,N-dimethylpropan-1-amine

Molecular formula: C20H21N

Molecular weight: 275.395 g/mol

Molecular structure:

2632 V pill chemistry

Drug class:  Cyclobenzaprine belongs to the class of organic molecules known as dibenzocycloheptenes which contains a dibenzocycloheptene moiety, that consists of two benzene rings connected by a cycloheptene ring.

2632 V pill uses

These pills are used as an adjunct to rest and physical therapy for relief of muscle spasm associated with acute, painful musculoskeletal conditions.

FDA approved indication

  • Acute muscle spasm

2632 v pill side effects

2632 V pill legal status

Cyclobenzaprine is not controlled substance. It is available only with a prescription.

What are different brand names for

Different brand names for cyclobenzaprine are:

  • Flexeril
  • Lisseril
  • Comfort Pac with Cyclobenzaprine
  • Fexmid

2632 V pill mechanism of action

Similarly to other tricyclic antidepressants, cyclobenzaprine also exhibits anticholinergic activity, norepinephrine potentiation, and antagonism of reserpine. It does not directly act on the neuromuscular junction or the muscle, however it relieves muscle spasms through a central action, likely at the brain stem level. Cyclobenzaprine also binds to the serotonin receptor sites and is considered as a 5-HT2 receptor antagonist that reduces muscle tone by decreasing the activity of descending serotonergic neurons.

2632 V pill pharmacokinetics

Absorption: 2632 V pills bioavailability range from 33% to 55%. Drug exhibits linear pharmacokinetics over the dose range 2.5 mg to 10 mg, and undergoes enterohepatic circulation.

Distribution: Cyclobenzaprine is highly bound to plasma proteins. It accumulates in the body when dosed 3 times a day, and will reach steady- state within 3-4 days.

Elimination: Cyclobenzaprine has an extensive metabolism, and is excreted primarily as glucuronides via the kidney. Cytochromes P-450 3A4, 1A2 enzymes and, to a lesser extent, 2D6, mediate N-demethylation, one of the oxidative pathways for cyclobenzaprine. The drug is eliminated quite slowly, with an effective elimination half-life of 18 hours and plasma clearance is 0.7 L/min.

2632 V pill side effects

Cyclobenzaprine may cause following side effects:

Common side effects:

  • Drowsiness
  • Dizziness
  • Dry mouth
  • Constipation
  • Fatigue

Serious side effects:

  • Fast or irregular heartbeat
  • Mood or mental changes (like confusion or hallucinations)
  • Trouble urinating
  • Chest pain
  • Fever
  • Seizures

Combining this drug with other antidepressant medications may lead to serotonin syndrome and can be fatal. Symptoms of serotonin syndrome include:

  • Confusion
  • Agitation or restlessness
  • Dilated pupils
  • Headache
  • Changes in blood pressure
  • Changes in body temperature
  • Nausea or vomiting
  • Severe diarrhea
  • Rapid heart rate
  • Loss of muscle coordination or twitching
  • Shivering or goosebumps
  • Heavy sweating

2632 V pill contraindications

Cyclobenzaprine is contraindicated in following situations:

  • Hypersensitivity reactions to any ingredient of this product.
  • Concomitant use of MAO inhibitors drugs or within 14 days after their discontinuation. There are some cases of hyperpyretic crisis seizures, and deaths that have occurred in patients receiving cyclobenzaprine concomitantly with MAO inhibitor drugs.
  • States after myocardial infarction
  • Diagnosed arrhythmias, heart block or conduction disturbances, or congestive heart failure.
  • Hypothyroidism

2632 V pill use during pregnancy

Cyclobenzaprine can be used during pregnancy only if clearly needed. It is scheduled in the US FDA pregnancy category B, which means that animal reproduction studies have failed to demonstrate a risk to the fetus and there are no adequate and well-controlled studies in women.

2632 V pill use during breastfeeding

As cyclobenzaprine is closely related to the tricyclic antidepressants, some of which are known to be excreted in human milk, it should be used with caution especially when other drugs that cause sedation are used simultaneously.

2632 V pill abuse and dependence

Because of cyclobenzaprine pharmacologic similarities with the tricyclic drugs, certain withdrawal symptoms should be considered when cyclobenzaprine is administered, even though they are not reported to occur with this drug. Abrupt cessation of treatment after long-term treatment rarely may produce nausea, headache, and malaise. Addiction as not been reported.

How long 2632 V pill stay in the system?

To determine how long 2632 V stays in the body after complete cessation, it is needed to consider its average elimination half-life time of about 18 hours.  This indicates that most cyclobenzaprine users will clear the drug form the body around 4.13 days after the final dose.  Though, it is always necessary to have in mind the fact that elimination half-life time can range from 8-37 hours, which may indicate that there’s significant interindividual variability in regards to excretion.

If patient has the fastest elimination of this drug with the half-life spectrum at 8 hours, it can be expected that the drug will be eliminated from their system in around 1.83 days (less than 48 hours).  Opposite, for patients on the slowest end of its half-life spectrum with 37 hours, it may take 8.48 days to fully eliminate cyclobenzaprine from their system.  The majority of users, elimination will take between 4 and 5 days after discontinuation.

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About Miljan Krcobic 300 Articles
Miljan Krčobić. has bachelor degree in Pharmacy.