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Lévonorgestrel (levonorgestrel)Version française

Medicine in DR Congo · official US FDA label

G-Nancy 1.5 mg

Lévonorgestrel (levonorgestrel) · comprimé

Authorized in DR Congo

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This is a US label.

The official US FDA label for levonorgestrel, effective September 1, 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 levonorgestrel

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

Uses

Use for women to reduce chance of pregnancy after unprotected sex (if a contraceptive failed or if you did not use birth control)

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 ■ take as soon as possible within 72 hours (3 days) after unprotected sex. The sooner you take it the better it will work. ■ if you vomit within 2 hours after taking the medication, call a healthcare professional to find out if you should repeat the dose

Warnings and precautions

Warnings Allergy alert: Do not use if you have ever had an allergic reaction to levonorgestrel Sexually transmitted diseases (STDs) alert: This product does not protect against HIV/AIDS or other STDs

Where to find it in DR Congo

Not in stock in our pharmacies right now

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Composition

SubstanceStrengthATC code
Lévonorgestrel (levonorgestrel)1.5 mg—

Marketing authorization in DR Congo

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

  • Authorization number

    M.S.1253/10/05/1261/2022

    Valid from July 26, 2022 until July 26, 2027

    Holder
    SUNGOLD LABORATOIRE Av du Rail, N ° 20, Q/ Kingabwa, commune de Limete, ville de Kinshasa, R.D Congo
    Manufacturer
    Alliance Biotech 440/3, Village Katha, Baddi, Distt. Solan (H.P.) - 173205 India
    Country
    R.D. Congo

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.