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

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Nortriptyline Hydrochloride

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

BOXED WARNING

Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults in short-term studies of major depressive disorder (MDD) and other psychiatric disorders. Anyone considering the use of nortriptyline hydrochloride or any other antidepressant in a child, adolescent, or young adult must balance this risk with the clinical need. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24; there was a reduction in risk with antidepressants compared to placebo in adults aged 65 and older. Depression and certain other psychiatric disorders are themselves associated with increases in teh risk of suicide. Patients of all ages who are started on antidepressant therapy should be monitored appropriately and observed closely for clinical worsening, suicidality, or unusual changes in behavior. Families and caregivers should be advised of the need for close observation and communication with the prescriber. Nortriptyline hydrochloride is not approved for use in pediatric patients. (See Warnings: Clinical Worsening and Suicide Risk,Precautions: Information for Patients, andPrecautions: Pediatric Use)


NORTRIPTYLINE HYDROCHLORIDE DESCRIPTION


Nortriptyline Hydrochloride





CLINICAL PHARMACOLOGY



INDICATIONS & USAGE



NORTRIPTYLINE HYDROCHLORIDE CONTRAINDICATIONS





WARNINGS

Clinical Worsening and Suicide Risk





All patients being treated with antidepressants for any indication should be monitored appropriately and observed closely for clinical worsening, suicidality, and unusual changes in behavior, especially during the initial few months of a course of drug therapy, or at times of dose changes, either increases or decreases.


Families and caregivers of patients being treated with antidepressants for major depressive disorder or other indications, both psychiatric and nonpsychiatric, should be alerted about the need to monitor patients for the emergence of agitation, irritability, unusual changes in behavior, and the other symptoms described above, as well as the emergence of suicidality, and to report such symptoms immediately to health care providers. Such monitoring should include daily observation by families and caregivers.
Screening Patients for Bipolar Disorder:





Use in Pregnancy


PRECAUTIONS

Information for Patients



Clinical Worsening and Suicide Risk







DRUG INTERACTIONS





Drugs Metabolized by P450 2D6




PEDIATRIC USE

BOX WARNINGWARNINGSClinical Worsening and Suicide Risk

GERIATRIC USE

DOSAGE AND ADMINISTRATION

NORTRIPTYLINE HYDROCHLORIDE ADVERSE REACTIONS

Note:
Cardiovascular
Psychiatric
Neurologic
Anticholinergic
Allergic
Hematologic -
Gastrointestinal
Endocrine
Other
Withdrawal Symptoms -

OVERDOSAGE



Manifestations

ADVERSE REACTIONS

Management
General


Gastrointestinal Decontamination

Cardiovascular


CNS


Psychiatric Follow


Pediatric Management


DOSAGE & ADMINISTRATION




Usual Adult Dose
Elderly and Adolescent Patients -

HOW SUPPLIED






STORAGE AND HANDLING




SPL MEDGUIDE






  • ●     all risks and benefits of treatment with antidepressant medicines
  • ●     all treatment choices for depression or other serious mental illness




  • ●               Pay close attention to any changes, especially sudden changes, in mood, behaviors, thoughts, or feelings. This is very important when an antidepressant medicine is started or when the dose is changed.
  • ●               Call the healthcare provider right away to report new or sudden changes in mood, behavior, thoughts, or feelings.
  • ●               Keep all follow-up visits with the healthcare provider as scheduled. Call the healthcare provider between visits as needed, especially if you have concerns about symptoms.

  • ●     thoughts about suicide or dying
  • ●     attempts to commit suicide
  • ●     new or worse depression
  • ●     new or worse anxiety
  • ●     feeling very agitated or restless
  • ●     panic attacks
  • ●     trouble sleeping (insomnia)
  • ●     new or worse irritability
  • ●     acting aggressive, being angry, or violent
  • ●     acting on dangerous impulses
  • ●     an extreme increase in activity and talking (mania)
  • ●     other unusual changes in behavior or mood

  • ●     Never stop an antidepressant medicine without first talking to a healthcare provider. Stopping an antidepressant medicine suddenly can cause other symptoms.
  • ●     Antidepressants are medicines used to treat depression and other illnesses. It is important to discuss all the risks of treating depression and also the risks of not treating it. Patients and their families or other caregivers should discuss all treatment choices with the healthcare provider, not just the use of antidepressants.
  • ●     Antidepressant medicines have other side effects. Talk to the healthcare provider about the side effects of the medicine prescribed for you or your family member.
  • ●     Antidepressant medicines can interact with other medicines. Know all of the medicines that you or your family member takes. Keep a list of all medicines to show the healthcare provider. Do not start new medicines without first checking with your healthcare provider.
  • ●     Not all antidepressant medicines prescribed for children are FDA approved for use in children. Talk to your child's healthcare provider for more information.



PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Nortriptyline Hydrochloride

Nortriptyline Hydrochloride

Nortriptyline Hydrochloride

Nortriptyline Hydrochloride CAPSULE

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-524(NDC:0591-5786)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
NORTRIPTYLINE HYDROCHLORIDE NORTRIPTYLINE 10 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
MAGNESIUM STEARATE
SODIUM LAURYL SULFATE
GELATIN
METHYLPARABEN
PROPYLPARABEN
titanium dioxide
BENZYL ALCOHOL
BUTYLPARABEN
edetate calcium disodium
sodium propionate
D&C YELLOW NO. 10
FD&C BLUE NO. 1
STARCH, CORN

Product Characteristics

Color Size Imprint Code Shape
white 16 mm NORTRIPTYLINE;DAN;10;mg CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-524-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA073553 2011-09-21


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