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Medicine in DR Congo · official US FDA label

Cimétidine 200 mg/2ml

Cimétidine (cimetidine) · solution injectable

Authorized in DR Congo

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This is a US label.

The official US FDA label for cimetidine, effective August 18, 2026, describes products sold in the United States. The medicine sold in DR Congo may differ in strength, form or approved uses: ask a pharmacist or a doctor.

Official US FDA label for cimetidine

Data provided by the U.S. Food and Drug Administration (openFDA), unchanged. The full label on DailyMed.

Uses

Uses • relieves heartburn associated with acid indigestion and sour stomach • prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages

Dosage

US dosage, for products sold in the United States. For a medicine bought in DR Congo, follow its box, its leaflet or your pharmacist.

Directions • adults and children 12 years and over: • to relieve symptoms, swallow 1 tablet with a glass of water • to prevent symptoms, swallow 1 tablet with a glass of water right before or any time up to 30 minutes before eating food or drinking beverages that cause heartburn • do not take more than 2 tablets in 24 hours • children under 12 years: ask a doctor

Warnings and precautions

Warnings Allergy alert: Do not use if you are allergic to cimetidine or other acid reducers Do not use • if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor. • with other acid reducers Ask a doctor before use if you have • frequent chest pain • frequent wheezing, particularly with heartburn • unexplained weight loss • nausea or vomiting • stomach pain • had heartburn over 3 months. This may be a sign of a more serious condition. • heartburn with lightheadedness, sweating or dizziness • chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness • kidney disease • liver disease Ask a doctor or pharmacist before use if you are taking • a prescription drug. Acid reducers may interact with certain prescription drugs. Stop use and ask a doctor if • you need to take this product for more than 14 days • stomach pain continues • your heartburn continues or worsens 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 (1-800-222-1222).

Where to find it in DR Congo

Not in stock in our pharmacies right now

Stock changes with every sale. Search by substance: a medicine with the same composition may be available.

Composition

SubstanceStrengthATC code
CIMÉTIDINE (cimetidine)200 mg/2ml—

Marketing authorization in DR Congo

From the register of the ACOREP (the Congolese pharmaceutical regulatory authority).

  • Authorization number

    MS1253/10/05/01750/2022

    Valid from October 11, 2022 until October 11, 2027

    Holder
    PLANET PHARMA Av. Lomami n°17 Q/Makutano, commune de Lubumbashi, ville de Lubumbashi, Haut-Katanga
    Manufacturer
    Anhui Chengshi Pharmaceutical Co.Ltd N° 5068 Huaishang road Bengbu, Anhui Province/China
    Country
    Chine
  • Authorization number

    MS.1253/10/05/DGM/0956/2021

    Valid from July 5, 2021 until July 5, 2026

    Holder
    MEDICO PLUS Av. Marché n° 1106, commune de Gombe, ville de Kinshasa, R.D Congo
    Manufacturer
    Anhui Chengshi Pharma Co. Ltd. N° 5068 Huaishang Road, Bengbu, Anhui province,China
    Country
    Chine
  • Authorization number

    MS.1253/10/05/DGM/0067/2021

    Valid from January 21, 2021 until January 21, 2026

    Holder
    MEDICO PLUS Av. Marché n° 1106, commune de Gombe, ville de Kinshasa, R.D Congo
    Manufacturer
    Tianjin Kingyork Group Hubei Tianyao Pharma Co. Ltd N°99 Hianjiang Bei Road, Xiangyang, Hubei/ P.R.China
    Country
    Chine

Sources

  • ●Labels: U.S. Food and Drug Administration, openFDA (public domain). Data provided by the U.S. Food and Drug Administration (openFDA), unchanged. DailyMed.
  • ●English names of substances: RxNorm, U.S. National Library of Medicine.
  • ●Marketing authorizations: register of the ACOREP, DR Congo, version of February 4, 2026.

Public information, for reference only: it does not replace the advice of a pharmacist or a doctor. Vimpia writes nothing about how to use a medicine and translates nothing: the label is the US FDA's, unchanged; names, composition and authorizations come from the official sources above.