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Meclizine 25 by The Generic Pharmaceutical Company

Medically reviewed on January 9, 2017

Dosage form: tablet
Labeler: The Generic Pharmaceutical Company
NDC Code: 57963-101

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Meclizine 25

Drug Facts

Active Ingredients (in each immediate-release tablet)

Meclizine 25 mg



Indications and Usage
  • For prevention and treatment of these symptoms associated with motion sickness:
    • nausea
    • vomiting
    • dizziness

  • Do not use for children under 12 years of age unless directed by a doctor.

Ask a doctor before use if you have
  • glaucoma
  • difficulty in urination due to enlargement of the prostate gland
  • a breathing problem such as emphysema or chronic bronchitis

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers

When using this product
  • drowsiness may occur
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery

If pregnant or breast-feeding,

  • ask health professional before use.

Keep out of reach of children.

In case of accidental overdose, seek medical help or contact a Poison Control Center immediately. 1-800-222-1222


Do not exceed recommended dosage.

To prevent motion sickness; take the first dose one hour before starting activity.

Adults and children 12 years of age and over:1 to 2 tablets once daily, or as directed by a doctor.

Inactive ingredients

Magnesium Stearate, Microcrystalline Cellulose, Sodium Starch Glycolate

Questions and comments?

Call 1-205-313-8298

Manufactured for
The Generic Pharmaceutical Company, Inc.
Leeds, AL 35094

PRINCIPAL DISPLAY PANEL - 25 mg Tablet Bottle Label

NDC 57963-101-01
100 Tablets

Meclizine 25

Each immediate-release tablet contains:
Meclizine HCl
25 mg

Store at 59°-86°F (15°-30°C)
[see USP Controlled Room Temperature].
Tamper evident by foil seal under cap.
Do not use if foil seal is broken or missing.

Manufactured for
The Generic Pharmaceutical Company, Inc.
Leeds, AL 35094

meclizine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57963-101
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
Magnesium Stearate 
Microcrystalline Cellulose 
Product Characteristics
ColorWHITEScoreno score
FlavorImprint CodeMC
#Item CodePackage Description
1NDC:57963-101-01100 TABLET in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart33612/01/2016
Labeler - The Generic Pharmaceutical Company (078787060)

The Generic Pharmaceutical Company

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.