Product image of Labella (Levonorgestrel) supplied by GNH India

Labella

Active Ingredient:
Levonorgestrel
Origin:
EU

Labella (Levonorgestrel)

Levonorgestrel, the active ingredient in Labella, is a progestin presented as an oral tablet for oral use. It is employed for emergency contraception and for the ongoing prevention of pregnancy in women of reproductive age by inhibiting ovulation and altering the uterine environment.

GNH India supplies Labella as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides reliable global distribution, ensuring product integrity throughout the supply chain.

Manufacturer / TM Owner

Uab Exeltis Baltics

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Indications & Clinical Uses

Levonorgestrel is a progestin used in hormonal contraceptive pathways.

  • Emergency contraception: prevents pregnancy when taken within 72‑120 hours after unprotected intercourse.
  • Regular contraception: used as a single‑dose or part of a hormonal regimen to provide ongoing pregnancy prevention.
  • Hormonal contraceptive for women of reproductive age: offers a progestin‑only option for those who cannot use estrogen‑containing methods.

How It Works

  • Levonorgestrel binds to progesterone receptors in the hypothalamus and pituitary, suppressing the luteinizing hormone surge and thereby inhibiting ovulation. It also induces changes in cervical mucus, reduces tubal motility, and alters the endometrial lining, creating an environment that is unfavorable for fertilization and implantation.

Side Effects

Levonorgestrel may cause a range of adverse reactions.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: transient cranial discomfort.
  • Abdominal pain: cramping or discomfort in the lower abdomen.
  • Menstrual changes: spotting, early or delayed periods.
  • Dizziness: brief episodes of light‑headedness.
  • Fatigue: feeling unusually tired.

Serious or Rare Side Effects

  • Severe allergic reaction: rash, swelling, or difficulty breathing.
  • Chest pain: may indicate cardiovascular involvement.
  • Severe abdominal pain: could signal ectopic pregnancy.
  • Liver dysfunction: jaundice or abnormal liver tests.
  • Vision changes: blurred or double vision.

Precautions & Warnings

Levonorgestrel should be used with attention to specific safety considerations.

  • Pregnancy contraindication: avoid use if already pregnant.
  • Hepatic impairment: use with caution in patients with liver disease.
  • Hypersensitivity: discontinue if allergic reaction occurs.
  • Breast cancer: not recommended for women with active estrogen‑dependent tumors.
  • Drug interactions: consider potential reduction of efficacy with enzyme‑inducing agents.
  • Store at room temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Levonorgestrel may interact with other medicines, affecting its effectiveness.

Major Interactions (Avoid)

  • Rifampicin: strong enzyme inducer that can markedly reduce contraceptive efficacy.
  • St. John’s wort: herbal inducer that may diminish hormonal activity.

Moderate Interactions (Monitor Closely)

  • Antifungal azoles (e.g., ketoconazole): may alter hormone metabolism.
  • Antiretroviral efavirenz: can decrease contraceptive effectiveness.
  • Anticonvulsants (e.g., phenytoin): may modestly reduce levonorgestrel levels.

Frequently Asked Questions

Labella contains levonorgestrel, a progestin that is used for emergency contraception after unprotected sexual intercourse and as a regular hormonal method to prevent pregnancy in women of reproductive age.

Levonorgestrel binds to progesterone receptors, suppressing the luteinizing hormone surge and preventing ovulation. It also thickens cervical mucus, reduces tubal motility, and alters the endometrium, making it difficult for fertilization and implantation to occur.

The specific dose and regimen of Labella are determined by the prescribing healthcare professional based on the indication and patient characteristics. Patients should follow the prescriber’s instructions and not alter the dose on their own.

Labella is intended to prevent pregnancy and should not be used by women who are already pregnant. Limited data are available for breastfeeding; however, levonorgestrel is excreted in small amounts in breast milk, and the benefits and risks should be discussed with a healthcare provider.

To order Labella, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Labella’s active ingredient, levonorgestrel, is a widely used progestin that offers effective pregnancy prevention when taken within 72‑120 hours. Compared with copper IUDs, it is less invasive but has a shorter window of efficacy; compared with ulipristal acetate, it may be slightly less effective beyond 72 hours but is more widely available.

Labella tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.

Labella is taken orally as a tablet. For emergency use, the tablet is swallowed with water as soon as possible after unprotected intercourse, following the prescriber’s timing guidance. For regular contraception, the dosing schedule is defined by the healthcare provider.

Serious risks, though rare, include severe allergic reactions (anaphylaxis), chest pain indicating possible cardiovascular events, severe abdominal pain that may signal an ectopic pregnancy, and significant liver dysfunction. Patients should seek immediate medical attention if any of these symptoms occur.

Labella should not be used by women who are already pregnant, have known hypersensitivity to levonorgestrel, have active breast cancer, or have severe liver disease. Individuals taking certain enzyme‑inducing medications should consult their provider, as efficacy may be reduced.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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