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

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Meclizine Hydrochloride

Sandoz Inc

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Meclizine hydrochloride, USP 12.5 mg

Meclizine hydrochloride, USP 25 mg

Purpose

Antiemetic

Meclizine Hydrochloride Uses

For prevention and treatment of these symptoms associated with motion sickness

  • nausea
  • vomiting
  • dizziness

Warnings

Ask a doctor before use if you have

  • a breathing problem such as emphysema or chronic bronchitis
  • glaucoma
  • difficulty in urination due to enlargement of the prostate gland

Ask a doctor or pharmacist before use if you are

  • giving this product to children under 12 years of age
  • taking sedatives or tranquilizers

When using this product

  • you may get drowsy
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • avoid alcoholic drinks
  • be careful when driving a motor vehicle or operating machinery

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

  • take first dose one hour before starting activity
  • adults and children (12 years and over) 25 to 50 mg (2 to 4 tablets) once daily or as directed by a doctor
  • not more than 4 tablets in 24 hours

Other Information

  • Safety sealed: do not use if the imprinted bottle seal is open or torn.
  • Keep tightly closed
  • Store at 20°-25°C (68°-77°F) (see USP Controlled Room Temperature).

Inactive ingredients

Croscarmellose sodium, FD&C blue #1 aluminum lake, hydroxypropyl methylcellulose, lactose (monohydrate), magnesium stearate, microcrystalline cellulose and polysorbate 80

Questions or comments?

1-800-525-8747

Sandoz Inc.

Princeton, NJ 08540

10-2008M

12.5 mg Label

NDC 0781-1345-01

Meclizine HCl

Tablets, USP

12.5 mg

Antiemetic

Relief of:

Nausea Vomiting Dizziness

100 Tablets

SANDOZ

25 mg Label

NDC 0781-1375-01

Meclizine HCl

Tablets, USP

25 mg

Antiemetic

Relief of:

Nausea Vomiting Dizziness

100 Tablets

SANDOZ

Meclizine Hydrochloride

Meclizine Hydrochloride TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0781-1345
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MECLIZINE HYDROCHLORIDE MECLIZINE 12.5 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
HYPROMELLOSES
lactose monohydrate
MAGNESIUM STEARATE
cellulose, microcrystalline
polysorbate 80
FD&C BLUE NO. 1

Product Characteristics

Color Size Imprint Code Shape
BLUE 5 mm GG;141 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0781-1345-01 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part336 1989-05-22


Meclizine Hydrochloride

Meclizine Hydrochloride TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0781-1375
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MECLIZINE HYDROCHLORIDE MECLIZINE 25 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
HYPROMELLOSES
lactose monohydrate
MAGNESIUM STEARATE
cellulose, microcrystalline
polysorbate 80
D&C YELLOW NO. 10
FD&C YELLOW NO. 6

Product Characteristics

Color Size Imprint Code Shape
YELLOW 6 mm GG;261 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0781-1375-01 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part336 1989-05-22


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Be sure to consult your doctor before taking any medication!
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