EContra One-Step

(Levonorgestrel) Tablet, 1.5 mg

Please see Product Information here.

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EContra One-Step is an OTC emergency contraceptive

Other 1.5 mg levonorgestrel emergency contraceptive products which include Plan B One-Step®, EContra® EZ, My Way®, AfterPill®, Fallback Solo, Opcicon One-Step, and Aftera®
  • Effective up to 3 days after unprotected sex or contraceptive failure
Product Gallery
ndc # package size order numbers
50102-211-16 Box Containing 6 Monocartons
ndc # 50102-211-16
package size Box Containing
6 Monocartons
order numbers

ORDER EContra One-Step

AMERISOURCEBERGEN

1-610-727-7000
www.amerisourcebergen.com
10186363

ANDA

1-800-331-2632 (Ext. 74591)
www.andanet.com
328092

CARDINAL

1-800-326-6457
www.cardinal.com
5439013

R&S NORTHEAST

1-800-262-7770
www.rsnortheast.com
021116

SEACOAST MEDICAL LLC

1-877-410-0811
www.seacoastmedical.com/afaxys
500041

SMITH MEDICAL PARTNERS LLC

1-800-292-9653
340B 1-877-445-7970
www.smpspecialty.com

571-2369

Product Information

USAGE

EContra One-Step (Levonorgestrel 1.5 mg tablet) is a progestin-only emergency contraceptive pill indicated for use in women to reduce the chance of pregnancy after unprotected sex (if contraceptive failed or birth control not used). EContra One-Step is not intended to be used in place of routine birth control.

WHO SHOULD NOT USE ECONTRA ONE-STEP
  • Women who are known to be pregnant as it will not work. However, EContra One-Step will not harm an existing pregnancy.
  • Women known to be allergic to Levonorgestrel.

Women should ask a doctor or pharmacist before using EContra One-Step if taking efavirenz (HIV medication) or rifampin (tuberculosis treatment) or medication for seizures (epilepsy). These medications may reduce the effectiveness of levonorgestrel.

Side effects may include:
  • Menstrual changes
  • Abdominal pain
  • Nausea or vomiting
  • Tiredness
  • Headache
  • Dizziness
  • Breast pain

Reference:
EContra One-Step [product information]. Charleston, SC: Afaxys Pharma, LLC; November 2017.

Please see full Product Information here.

To report SUSPECTED ADVERSE REACTIONS, call 1-855-888-2467 or report via the FDA MedWatch Program at www.fda.gov/medwatch or 1-800-FDA-1088.