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Molecule

Norethindrone

Also known as norethindrone acetate
Available on request
Presentations
14
Brands
12
Manufacturers
8
Available from stock
0

Norethindrone is a progestin indicated for the prevention of pregnancy. It is available as tablets for oral use. MedsAcross supplies Norethindrone for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Progestin
ATC classification
G03AC01 Norethindrone · Contraceptive agents, subgroup G03ACG03DC02 Norethindrone · Sex hormones and fertility medicines, subgroup G03D, subgroup G03DC
US FDA first approval
2 January 1973
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Oral
Dosage forms
Tablet
Identifiers
UNII T18F433X4SRxCUI 7514CAS 68-22-4DrugBank DB00717Q421352

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

1. Indications. Progestin-only oral contraceptives are indicated for the prevention of pregnancy. 2. Efficacy. If used perfectly, the first-year failure rate for progestin-only oral contraceptives is 0.5%. However, the typical failure rate is estimated to be closer to 5%, due to late or omitted pills. The following table lists the pregnancy rates for users of all major methods of contraception. Table 2: Percentage of Women Experiencing an Unintended Pregnancy During the First Year of Typical Use and the First Year of Perfect Use of Contraception and the Percentage Continuing Use at the End of the First Year. United States. % of Women Experiencing an Unintended Pregnancy within the First Year of Use % of Women Continuing Use at One Year 3 Method. Typical Use 1. Perfect Use 2.

Source: US FDA prescribing information

Dosing overview

To achieve maximum contraceptive effectiveness, Nora-BE must be taken exactly as directed. One tablet is taken every day, at the same time. Administration is continuous, with no interruption between pill packs. See PATIENT LABELING for detailed instructions.

Source: US FDA prescribing information

Contraindications

Progestin-only oral contraceptives (POPs) should not be used by women who currently have the following conditions: Known or suspected pregnancy Known or suspected carcinoma of the breast Undiagnosed abnormal genital bleeding Hypersensitivity to any component of this product Benign or malignant liver tumors Acute liver disease

Source: US FDA prescribing information

Warnings and precautions

Cigarette smoking greatly increases the possibility of suffering heart attacks and strokes. Women who use oral contraceptives are strongly advised not to smoke. Nora-BE does not contain estrogen and, therefore, this insert does not discuss the serious health risks that have been associated with the estrogen component of combined oral contraceptives. The health care provider is referred to the prescribing information of combined oral contraceptives for a discussion of those risks, including, but not limited to, an increased risk of serious cardiovascular disease in women who smoke, carcinoma of the breast and reproductive organs, hepatic neoplasia, and changes in carbohydrate and lipid metabolism.

Source: US FDA prescribing information

Side effects

Menstrual irregularity is the most frequently reported side effect. Frequent and irregular bleeding are common, while long duration of bleeding episodes and amenorrhea are less likely. Headache, breast tenderness, nausea, and dizziness are increased among progestin-only oral contraceptive users in some studies. Androgenic side effects such as acne, hirsutism, and weight gain occur rarely.

Source: US FDA prescribing information

Interactions

4. Drug interactions. Change in contraceptive effectiveness associated with co-administration of other products: a. Anti-infective agents and anticonvulsants. Contraceptive effectiveness may be reduced when hormonal contraceptives are co-administered with antibiotics, anticonvulsants, and other drugs that increase the metabolism of contraceptive steroids. This could result in unintended pregnancy or breakthrough bleeding. Examples include rifampin, barbiturates, phenylbutazone, phenytoin, carbamazepine, felbamate, oxcarbazepine, topiramate, and griseofulvin. b. Anti-HIV protease inhibitors. Several of the anti-HIV protease inhibitors have been studied with co-administration of oral contraceptives, significant changes (increase and decrease) in the plasma levels of the estrogen and progestin have been noted in some cases.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

14 presentations of Norethindrone, sorted by availability.

MedicineManufacturerRegisterAvailability
Norethindrone 5 mg tabletOralGeneric name—US FDAAvailable on request
Norethindrone 0.35 mg tabletOralGeneric name—US FDAAvailable on request
Incassia 0.35 mg tabletOralAurobindo PharmaIndiaUS FDAAvailable on request
Emzahh 0.35 mg tabletOralAurobindo PharmaIndiaUS FDAAvailable on request
Errin 0.35 mg tabletOralDr. Reddy's LaboratoriesIndiaUS FDAAvailable on request
Affodel 0.35 mg tabletOralNaariUS FDAAvailable on request
Camila 0.35 mg tabletOralDr. Reddy's LaboratoriesIndiaUS FDAAvailable on request
Gallifrey 5 mg tabletOralXiromedUS FDAAvailable on request
Jencycla 0.35 mg tabletOralLupinIndiaUS FDAAvailable on request
Lyleq 0.35 mg tabletOralAfaxys PharmaUS FDAAvailable on request
Meleya 0.35 mg tabletOralXiromedUS FDAAvailable on request
Nora BE 0.35 mg tabletOralTeva PharmaceuticalsUS FDAAvailable on request
Orquidea 0.35 mg tabletOralXiromedUS FDAAvailable on request
Heather 0.35 mg tabletOralGlenmark PharmaceuticalsIndiaUS FDAAvailable on request

Brands by market

12 brand names across 1 markets.

Brand names by country

Manufacturers

Indian manufacturers are highlighted.

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 2 January 1973Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Norethindrone in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Norethindrone available for export from India?

Yes, on request. MedsAcross lists 14 presentations of Norethindrone and sources them for licensed hospitals, importers and physicians against valid import documents. Indian manufacturers include Aurobindo Pharma, Dr. Reddy's Laboratories, Glenmark Pharmaceuticals.

What brand names does Norethindrone have?

The catalogue lists 12 brand names for Norethindrone, including Affodel, Camila, Emzahh, Errin, Gallifrey, Heather, Incassia, Jencycla.

Is Norethindrone approved by the US FDA?

Yes. The US FDA first approved Norethindrone on 2 January 1973, according to Drugs@FDA.

Does Norethindrone need cold chain shipping?

No listed presentation of Norethindrone is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

Which ATC class is Norethindrone in?

Norethindrone is classified under ATC code G03AC01 (Norethindrone).

References

  1. Nora BE prescribing information (Teva Pharmaceuticals). U.S. National Library of Medicine, DailyMed. Retrieved 28 February 2022

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