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You are here: Home » eGM Resources » Health Information & Resources Portal|Home » RX Drug List (listed alphabetically) » Drug Reference (M's) » Metoclopramide



DESCRIPTION

Metoclopramide hydrochloride is a white crystalline, odorless substance, freely soluble in water. Chemically it is 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-methoxy benzamide monohydrochloride monohydrate. Molecular weight: 354.3.

FOR ORAL ADMINISTRATION

Reglan Tablets (Metoclopramide Tablets, USP) 10 mg are white, scored, capsule-shaped tablets engraved Reglan on one side and AHR 10 on the opposite side.

Each tablet contains:

    Metoclopramide base...........................10 mg
    (as the monohydrochloride monohydrate)

Inactive Ingredients: Magnesium Stearate, Mannitol, Microcrystalline Cellulose, Stearic Acid.

Reglan Tablets (Metoclopramide Tablets, USP) 5 mg are green elliptical-shaped tablets engraved Reglan 5 on one side and AHR on the opposite side.

Each tablet contains:

    Metoclopramide base...........................5 mg
    (as the monohydrochloride monohydrate)

Inactive Ingredients: Corn Starch, D&C Yellow 10 Lake, FD&C Blue 1 Aluminum Lake, Lactose, Microcrystalline Cellulose, Silicon Dioxide, Stearic Acid.

Reglan Syrup (Metoclopramide Oral Solution, USP) is an orange-colored, palatable, aromatic, sugar-free liquid.

Each 5 mL (1 teaspoonful) contains:

    Metoclopramide base...........................5 mg
    (as the monohydrochloride monohydrate)

Inactive Ingredients: Citric Acid, FD&C Yellow 6, Flavors, Glycerin, Methylparaben, Propylparaben, Sorbitol, Water.

FOR PARENTERAL ADMINISTRATION

Reglan Injectable (Metoclopramide Injection, USP) is a clear, colorless, sterile solution with a pH of 4.5-6.5 for intravenous or intramuscular administration.
CONTAINS NO PRESERVATIVE.
2 mL and 10 mL single dose vials; 2 mL single dose ampuls; 30 mL single dose vial

Each 1 mL contains:

    Metoclopramide base...........................5 mg
    (as the monohydrochloride monohydrate)

Sodium Chloride, USP 8.5 mg, Water for Injection USP q.s. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide.





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