EContra® EZ

(Levonorgestrel) Tablet, 1.5 mg

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EContra® EZ is an AB-Rated emergency contraceptive

Reference Drug: Plan B One-Step®

Compares to: Take Action®, Next Choice One Dose ®, My Way®, AfterPill ®, Fallback Solo ®, Opcicon® One-Step and Aftera™, Morning After, Option 2®
  • Launched March 2015
  • Effective up to three days after unprotected sex or contraceptive failure
Product Gallery
ndc # package size pi order numbers product info sheet
50102-111-01 Monocarton Containing
1-tablet Blister Pack
50102-111-12 Box Containing
12 Monocartons

ORDER EContra® EZ

AmerisourceBergen

1-610-727-7000
www.amerisourcebergen.com
10157388

ANDA

1-800-331-2632 (Ext. 74591)
www.andanet.com
501490

Cardinal

1-800-326-6457
www.cardinal.com
5062591

R&S Northeast

1-800-262-7770
www.rsnortheast.com
011112

Seacoast Medical LLC

1-877-410-0811
www.seacoastmedical.com/afaxys
500015

Smith Medical Partners LLC

1-800-292-9653
340B 1-877-445-7970 www.smpspecialty.com
541-0949

Product Information

USAGE

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

WHO SHOULD NOT USE ECONTRA EZ

Women who are known to be pregnant as it will not work. However, EContra EZ will not harm an existing pregnancy.

Women known to be allergic to levonorgestrel.

SIDE EFFECTS MAY INCLUDE:
  • Menstrual changes. After EContra EZ women may experience heavier or lighter bleeding. If the next period is more than a week late, consider pregnancy.
  • Abdominal pain. Ectopic pregnancy should be considered in cases of severe abdominal pain.
  • Nausea or vomiting. If women vomit within 2 hours of taking the medication, consider recommending a second dose.
  • Tiredness
  • Headaches
  • Dizziness
  • Breast Pain
  • Hypersensitivity to any of the components of levonorgestrel and ethinyl estradiol tablets

Reference: EContra® EZ product information. Charleston, SC: Afaxys, Inc. August 2016.

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.