Optionelle

LEVONORGESTREL TABLET, 1.5 MG ORAL HUMAN OTC DRUG

Optionelle is an FDA drug label for the active ingredient LEVONORGESTREL TABLET, 1.5 MG manufactured by Strides Pharma Inc administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20220916.

Generic name
LEVONORGESTREL TABLET, 1.5 MG
Manufacturer
Strides Pharma Inc
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
59556-286
Application
ANDA202380
Label effective
20220916

About this product

Optionelle is an FDA-registered drug product whose active ingredient is LEVONORGESTREL TABLET, 1.5 MG. It is labelled by Strides Pharma Inc taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 59556-286, application ANDA202380, label effective 20220916. It is one of 2 FDA drug label records sharing the active ingredient LEVONORGESTREL TABLET, 1.5 MG. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing LEVONORGESTREL TABLET, 1.5 MG are most often described in connection with: women reduce, chance pregnancy, unprotected sex, contraceptive failed, birth control. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient Levonorgestrel 1.5 mg

Indications & Usage

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

Dosage & Administration

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

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

More products with the same ingredient

LEVONORGESTREL TABLET, 1.5 MG

Levonorgestrel Tablet, 1.5 mg

Strides Pharma Inc View label

How products containing LEVONORGESTREL TABLET, 1.5 MG compare

FDA lists 2 drug label records with LEVONORGESTREL TABLET, 1.5 MG as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — Strides Pharma Inc 2
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Recall and safety notices

5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

RecallProductFirmClassStatusReported
D-0390-2026 Children's Ibuprofen Oral Suspension, USP, 100 mg per 5mL, 4 FL OZ (120 mL) bottle, Manufactured for: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, Made in India, NDC 51672-5321-8. STRIDES PHARMA INC Class II Ongoing 20260325
D-0260-2024 Methoxsalen Capsules, USP 10mg, 50-count bottle, Rx Only, Manufactured by: Strides Pharma Science Ltd. Bengaluru - 562106, India. Distributed by:Strides Pharma Inc. East Brunswick, NJ 08816, NDC 64380-752-16 Strides Pharma Inc. Class II Terminated 20240131
D-0895-2023 Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram- 603 110, Tamilnadu, India, NDC 64380-933-08 Strides Pharma Inc. Class II Terminated 20230712
D-1330-2022 Prednisone Tablets USP, 20 mg, 100-count bottle, Rx Only, Manufactured by: Strides Pharma Science Ltd., Bengaluru - 562106, India, Distributed by: Strides Pharma Inc., East Brunswick, NJ 08816, NDC 64380-785-06. Strides Pharma Inc. Class II Terminated 20220817
D-0973-2022 Losartan Potassium Tablets, USP, 50 mg, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No., 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India, Distributed by: Strides Pharma Inc., East Brunswick, NJ 08816. 90 film coated tablets NDC 64380-934-05 1000 film coated tablets NDC 64380-934-08 Strides Pharma Inc. Class II Terminated 20220608

Frequently asked questions

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

Who makes Optionelle?
Strides Pharma Inc is the labeler of record for Optionelle. 2 FDA label records share the active ingredient LEVONORGESTREL TABLET, 1.5 MG, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Optionelle come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Optionelle prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing LEVONORGESTREL TABLET, 1.5 MG?
Yes. 2 FDA drug label records list LEVONORGESTREL TABLET, 1.5 MG as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Optionelle been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.