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My Choice TM by Sun Pharmaceutical Industries Limited

Medically reviewed on June 18, 2018

Dosage form: tablet
Ingredients: LEVONORGESTREL 1.5mg
Labeler: Sun Pharmaceutical Industries Limited
NDC Code: 62756-720

My Choice™

Drug Facts

Active ingredient

Levonorgestrel, USP 1.5 mg

Purpose

Emergency contraceptive

Use

for women to reduce chance of pregnancy af ter unprotected sex (if a contraceptive failed or if you did not use bir th control)

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.

Do not use
  • if you are already pregnant (because it will not work)
  • for regular bir th control

Ask a doctor or pharmacist before use if you are taking efavirenz (HIV medication) or rifampin (tuberculosis treatment) or medication for seizures (epilepsy). These medications may reduce the effectiveness of levonorgestrel.

When using this product you may have

  • menstrual changes
  • tiredness
  • dizziness
  • nausea
  • headache
  • breast pain
  • lower stomach (abdominal) pain
  • vomiting

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

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

Other information
  • read the instructions, warnings, and enclosed product leaflet before use
  • this product works mainly by preventing ovulation (egg release). It may also prevent fer tilization of a released egg (joining of sperm and egg) or at tachment of a fer tilized egg to the uterus (implantation).
  • do not use if carton is open or tear strip is removed or blister seal is broken or missing
  • store at 20° to 25°C (68° to 77°F)

Inactive ingredients

colloidal silicon dioxide, corn starch, hypromellose, lactose monohydrate, magnesium stearate, talc

Questions or comments?

For more information, call toll free 1-800-818-4555 weekdays

Distributed by:
Ohm Laboratories Inc.
New Brunswick, NJ 08901

PRINCIPAL DISPLAY PANEL - 1.5 mg Tablet Blister Pack Carton

Compare To
the active ingredient of
Plan B One-Step
®

NDC 62756-720-60

See New Warning

My
Choice

Levonorgestrel Tablet 1.5 mg
Emergency Contraceptive

  • Reduces the chance of pregnancy after unprotected sex
  • Not for regular birth control
  • The sooner you take it, the more effective it will be
  • Take as soon as possible within 72 hours (3 days)
    after unprotected sex
  • Will not harm an existing pregnancy

1 Tablet Levonorgestrel 1.5 mg

One Tablet. One Step.

MY CHOICE TM 
levonorgestrel tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62756-720
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LEVONORGESTREL (LEVONORGESTREL) LEVONORGESTREL1.5 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE 
STARCH, CORN 
HYPROMELLOSE, UNSPECIFIED 
LACTOSE MONOHYDRATE 
MAGNESIUM STEARATE 
TALC 
Product Characteristics
ColorWHITE (white to off-white) Scoreno score
ShapeROUND (circular) Size8mm
FlavorImprint Code718
Contains    
Packaging
#Item CodePackage Description
1NDC:62756-720-601 BLISTER PACK in 1 CARTON
11 TABLET in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20263504/01/2018
Labeler - Sun Pharmaceutical Industries Limited (650172430)
Establishment
NameAddressID/FEIOperations
Sun Pharmaceutical Industries Limited725959238ANALYSIS(62756-720), MANUFACTURE(62756-720)

 
Sun Pharmaceutical Industries Limited

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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