Label: TIGAN(R)- TRIMETHOBENZAMIDE HYDROCHLORIDE injection

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated January 28, 2024

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  • SPL UNCLASSIFIED

    Injectable

    For Intramuscular Use Only

    Not for Use in Pediatric Patients

  • DESCRIPTION

    Chemically, trimethobenzamide hydrochloride (HCl) is N-[p-[2-(dimethylamino)ethoxy]benzyl]-3,4,5-trimethoxybenzamide monohydrochloride. It has a molecular weight of 424.93 and the following structural formula:

    STRUCTURE

    Single Dose Vials: Each 2-mL single-dose vial contains 200 mg trimethobenzamide hydrochloride compounded with 1 mg sodium citrate and 0.4 mg citric acid as buffers and pH adjusted to approximately 5.0 with sodium hydroxide.

    Multi-Dose Vials: Each mL contains 100 mg trimethobenzamide hydrochloride compounded with 0.45% phenol as preservative, 0.5 mg sodium citrate and 0.2 mg citric acid as buffers and pH adjusted to approximately 5.0 with sodium hydroxide.

  • CLINICAL PHARMACOLOGY

    Mechanism of Action

    The mechanism of action of Tigan® as determined in animals is obscure, but may involve the chemoreceptor trigger zone (CTZ), an area in the medulla oblongata through which emetic impulses are conveyed to the vomiting center; direct impulses to the vomiting center apparently are not similarly inhibited. In dogs pretreated with trimethobenzamide HCl, the emetic response to apomorphine is inhibited, while little or no protection is afforded against emesis induced by intragastric copper sulfate.

    Pharmacokinetics

    The pharmacokinetics of trimethobenzamide have been studied in healthy adult subjects. Following administration of 200 mg (100 mg/mL) Tigan IM injection, the time to reach maximum plasma concentration (Tmax) was about half an hour, about 15 minutes longer for Tigan 300 mg oral capsule than an IM injection. A single dose of Tigan 300 mg oral capsule provided a plasma concentration profile of trimethobenzamide similar to Tigan 200 mg IM. The relative bioavailability of the capsule formulation compared to the solution is 100%. The mean elimination half-life of trimethobenzamide is 7 to 9 hours. Between 30 – 50% of a single dose in humans is excreted unchanged in the urine within 48 – 72 hours. The metabolic disposition of trimethobenzamide in humans is not known. Specifically, it is not known if active metabolites are generated in humans.

    Special Populations

    Age

    The clearance of trimethobenzamide is not known in patients with renal impairment. However, it may be advisable to consider reduction in the dosing of trimethobenzamide in elderly patients with renal impairment considering that a substantial amount of excretion and elimination of trimethobenzamide occurs via the kidney and that elderly patients may have various degrees of renal impairment. (See PRECAUTIONS: GENERAL and DOSAGE AND ADMINISTRATION).

    Gender

    Systemic exposure to trimethobenzamide was similar between men (N=40) and women (N=28).

    Race

    Pharmacokinetics appeared to be similar for Caucasians (N=53) and African Americans (N=12).

    Renal Impairment

    The clearance of trimethobenzamide is not known in patients with renal impairment. However, it may be advisable to consider reduction in the dosing of trimethobenzamide in patients with renal impairment considering that a substantial amount of excretion and elimination of trimethobenzamide occurs via the kidney. (See PRECAUTIONS: GENERAL and DOSAGE AND ADMINISTRATION).

  • INDICATIONS

    Tigan® is indicated for the treatment of postoperative nausea and vomiting and for nausea associated with gastroenteritis.

  • CONTRAINDICATIONS

    The injectable form of Tigan® is contraindicated in pediatric patients and in patients with known hypersensitivity to trimethobenzamide.

  • WARNINGS

    Tigan® may produce drowsiness. Patients should not operate motor vehicles or other dangerous machinery until their individual responses have been determined.

    Usage in Pregnancy

    Trimethobenzamide hydrochloride was studied in reproduction experiments in rats and rabbits and no teratogenicity was suggested. The only effects observed were an increased percentage of embryonic resorptions or stillborn pups in rats administered 20 mg and 100 mg/kg and increased resorptions in rabbits receiving 100 mg/kg. In each study these adverse effects were attributed to one or two dams. The relevance to humans is not known. Since there is no adequate experience in pregnant or lactating women who have received this drug, safety in pregnancy or in nursing mothers has not been established.

    Usage with Alcohol

    Concomitant use of alcohol with Tigan® may result in an adverse drug interaction.

  • PRECAUTIONS

    During the course of acute febrile illness, encephalitides, gastroenteritis, dehydration and electrolyte imbalance, especially in children and the elderly or debilitated, CNS reactions such as opisthotonos, convulsions, coma and extrapyramidal symptoms have been reported with and without use of Tigan® (trimethobenzamide hydrochloride) or other antiemetic agents. In such disorders caution should be exercised in administering Tigan®, particularly to patients who have recently received other CNS-acting agents (phenothiazines, barbiturates, belladonna derivatives). Primary emphasis should be directed toward the restoration of body fluids and electrolyte balance, the relief of fever and relief of the causative disease process. Overhydration should be avoided since it may result in cerebral edema.

    The antiemetic effects of Tigan® may render diagnosis more difficult in such conditions as appendicitis and obscure signs of toxicity due to overdosage of other drugs.

    General

    Adjustment of Dose in Renal Failure

    A substantial route of elimination of unchanged trimethobenzamide is via the kidney. Dosage adjustment should be considered in patients with reduced renal function including some elderly patients. (See CLINICAL PHARMACOLOGY and DOSAGE AND ADMINISTRATION).

    Geriatric Use

    Clinical studies of trimethobenzamide hydrochloride did not include sufficient numbers of patients aged 65 and over to determine whether they respond differently from younger patients. Although there are studies reported in the literature that include elderly patients > 65 years old with younger patients, it is not known if there are differences in efficacy or safety parameters for elderly and non-elderly patients treated with trimethobenzamide. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.

    This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function. (See CLINICAL PHARMACOLOGY and DOSAGE AND ADMINISTRATION).

  • ADVERSE REACTIONS

    There have been reports of hypersensitivity reactions and Parkinson-like symptoms. There have been instances of hypotension reported following parenteral administration to surgical patients. There have been reports of blood dyscrasias, blurring of vision, coma, convulsions, depression of mood, diarrhea, disorientation, dizziness, drowsiness, headache, jaundice, muscle cramps and opisthotonos. If these occur, the administration of the drug should be discontinued. Allergic-type skin reactions have been observed; therefore, the drug should be discontinued at the first sign of sensitization. While these symptoms will usually disappear spontaneously, symptomatic treatment may be indicated in some cases.

    For medical advice about adverse reactions contact your medical professional. To report SUSPECTED ADVERSE REACTIONS, contact Par Pharmaceutical, Inc. at 1-800-828-9393 or FDA at 1-800-FDA-1088 (1-800-332-1088) or www.fda.gov/medwatch.

  • DOSAGE & ADMINISTRATION

    (See WARNINGS and PRECAUTIONS.)

    Dosage should be adjusted according to the indication for therapy, severity of symptoms and the response of the patient.

    Geriatric Patients

    Dose adjustment such as reducing the total dose administered at each dosing or increasing the dosing interval should be considered in elderly patients with renal impairment (creatinine clearance ≤ 70 mL/min/1.73m2). Final dose adjustment should be based upon integration of clinical efficacy and safety considerations. (See CLINICAL PHARMACOLOGY and PRECAUTIONS).

    Patients with Renal Impairment

    In subjects with renal impairment (creatinine clearance ≤ 70 mL/min/1.73m2), dose adjustment such as reducing the total dose administered at each dosing or increasing the dosing interval should be considered. (See CLINICAL PHARMACOLOGY and DOSAGE AND ADMINISTRATION).

    INJECTABLE, 100 mg/mL (Not for use in pediatric patients)
    Usual Adult Dosage
    2 mL (200 mg) t.i.d. or q.i.d. intramuscularly.

    NOTE: The injectable form is intended for intramuscular administration only; it is not recommended for intravenous use.

    Intramuscular administration may cause pain, stinging, burning, redness and swelling at the site of injection. Such effects may be minimized by deep injection into the upper outer quadrant of the gluteal region, and by avoiding the escape of solution along the route.

  • STORAGE

    Store between 20° to 25°C (68° to 77°F).

    (See USP Controlled Room Temperature.)

  • HOW SUPPLIED

    TIGAN(R) (TRIMETHOBENZAMIDE HYDROCHLORIDE) INJECTION is supplied in the following dosage forms.
    NDC 51662-1430-1
    TIGAN(R) (TRIMETHOBENZAMIDE HYDROCHLORIDE) INJECTION 200mg/2mL (100mg/mL) 2mL VIAL

    NDC 51662-1430-2
    TIGAN(R) (TRIMETHOBENZAMIDE HYDROCHLORIDE) INJECTION 200mg/2mL (100mg/mL) 2mL VIAL, 1 VIAL PER POUCH

    NDC 51662-1430-3
    TIGAN(R) (TRIMETHOBENZAMIDE HYDROCHLORIDE) INJECTION 200mg/2mL (100mg/mL) 2mL VIAL, 1 VIAL PER POUCH, 25 POUCHES PER CASE

    HF Acquisition Co LLC, DBA HealthFirst
    Mukilteo, WA 98275

  • SPL UNCLASSIFIED

    Rx Only

    Distributed by:
    Par Pharmaceutical
    Chestnut Ridge, NY 10977

    R04/16

    OS118J-01-90-02

    3000358G

  • PRINCIPAL DISPLAY PANEL - VIAL LABEL

    VIAL LABEL

  • PRINCIPAL DISPLAY PANEL - SERIALIZED LABELING

    SERIALIZED LABELING

  • PRINCIPAL DISPLAY PANEL NDC 51662-1430-2 POUCH LABELING

    NDC 51662-1430-2 POUCH LABELING

    POUCH

    VIAL LABELING

    VIAL LABEL

  • PRINCIPAL DISPLAY PANEL - NDC 51662-1430-3 CASE LABELING

    NDC 51662-1430-3 CASE LABELING

    Case Labeling

    SERIALIZED CASE RFID LABELING

    RFID Label

  • INGREDIENTS AND APPEARANCE
    TIGAN(R) (TRIMETHOBENZAMIDE HYDROCHLORIDE) 
    tigan(r) (trimethobenzamide hydrochloride) injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:51662-1430(NDC:42023-119)
    Route of AdministrationINTRAMUSCULAR
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRIMETHOBENZAMIDE HYDROCHLORIDE (UNII: WDQ5P1SX7Q) (TRIMETHOBENZAMIDE - UNII:W2X096QY97) TRIMETHOBENZAMIDE HYDROCHLORIDE100 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) 0.2 mg  in 1 mL
    SODIUM CITRATE (UNII: 1Q73Q2JULR) 0.5 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51662-1430-12 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product01/10/2020
    2NDC:51662-1430-325 in 1 CASE12/11/2022
    2NDC:51662-1430-21 in 1 POUCH
    22 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01753001/10/2020
    Labeler - HF Acquisition Co LLC, DBA HealthFirst (045657305)
    Registrant - HF Acquisition Co LLC, DBA HealthFirst (045657305)
    Establishment
    NameAddressID/FEIBusiness Operations
    HF Acquisition Co LLC, DBA HealthFirst045657305relabel(51662-1430)