Label: LOMAIRA- phentermine hydrochloride tablet

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: CIV
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated April 7, 2023

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  • DESCRIPTION
    Phentermine hydrochloride is a sympathomimetic amine anorectic. Its chemical name is α,α,-dimethylphenethylamine hydrochloride. The structural formula is as follows: Phentermine hydrochloride is ...
  • CLINICAL PHARMACOLOGY
    Mechanism of Action - Phentermine is a sympathomimetic amine with pharmacologic activity similar to the prototype drugs of this class used in obesity, amphetamine (d- and dll-amphetamine) ...
  • CLINICAL STUDIES
    In relatively short-term clinical trials, adult obese subjects instructed in dietary management and treated with “anorectic” drugs lost more weight on the average than those treated with placebo ...
  • INDICATIONS AND USAGE
    LOMAIRA™ tablets are indicated as a short-term (a few weeks) adjunct in a regimen of weight reduction based on exercise, behavioral modification and caloric restriction in the management of ...
  • CONTRAINDICATIONS
    • History of cardiovascular disease (e.g., coronary artery disease, stroke, arrhythmias, congestive heart failure, uncontrolled hypertension) • During or within 14 days ...
  • WARNINGS
    Coadministration with Other Drug Products for Weight Loss - LOMAIRA™ tablets are indicated only as short-term (a few weeks) monotherapy for the management of exogenous obesity. The safety and ...
  • PRECAUTIONS
    Information for Patients - Patients must be informed that phentermine hydrochloride is a short-term (a few weeks) adjunct in a regimen of weight reduction based on exercise, behavioral ...
  • ADVERSE REACTIONS
    The following adverse reactions are described, or described in greater detail, in other sections: - Primary pulmonary hypertension (see - Warnings) ...
  • DRUG ABUSE AND DEPENDENCE
    Controlled Substance - Phentermine is a Schedule IV controlled substance. Abuse - Phentermine is related chemically and pharmacologically to the amphetamines. Amphetamines and other ...
  • OVERDOSAGE
    The least amount feasible should be prescribed or dispensed at one time in order to minimize the possibility of overdosage. Acute Overdosage - Manifestations of acute overdosage include ...
  • DOSAGE AND ADMINISTRATION
    Dosage should be individualized to obtain an adequate response with the lowest effective dose. The usual adult dose is one tablet three times a day ½ hour before meals ...
  • HOW SUPPLIED/STORAGE AND HANDLING
    LOMAIRA™ is available as follows: LOMAIRA™ 8 mg is supplied as white butterfly shaped tablets with blue speckles, debossed “K1” on one side and bisected on the other side. Bottles of 30, NDC ...
  • Package Labeling:17224-840-28
    17224-840-28
  • Package Labeling:17224-840-60
    17224-840-60
  • Package Labeling:17224-840-90
    17224-840-90
  • INGREDIENTS AND APPEARANCE
    Product Information