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MINIVLAR 30

Medically reviewed by Drugs.com. Last updated on Nov 11, 2021.

Dosage form: tablet
Ingredients: ETHINYL ESTRADIOL 0.03mg, LEVONORGESTREL 0.15mg
Labeler: OASIS TRADING
NDC Code: 72689-0011

Ethinyl Estradiol, Levonorgestrel

Oral contraception

Keep out of reach of children

1 tab daily for 21 days; repeat.

Warnings/Precautions:
Smokers over 35yrs of age: not recommended. Uncontrolled hypertension. Hypertriglyceridemia. Discontinue if jaundice, visual disturbances, migraine or other severe headaches occur. Do regular complete physical exams. May need barrier contraception with Sunday starts or postpartum use (see literature). Nursing mothers: not recommended
Contraindications
Thrombophlebitis or thromboembolic disorders. Cerebral vascular or coronary artery disease. Breast or other estrogen-dependent neoplasms. Undiagnosed abnormal genital bleeding. Cholestatic jaundice of pregnancy or jaundice with prior OC use. Hepatic adenoma or carcinoma. Pregnancy (Cat.X).
Interactions
Antagonized by hepatic enzyme inducing drugs (eg, rifampin, griseofulvin, St. John's wort), possibly others. May affect measurement of sex hormone-binding globulin levels
Adverse Reactions:
Hypertension, nausea, vomiting, breakthrough bleeding, amenorrhea, transient delay of ovulation after discontinuation, edema, chloasma, mastodynia, headache, intolerance to contact lenses. Increased risk of gallbladder disease, thromboembolic disorders.

Stearic acid, corn starch, polyethylene glycol 6000

For oral use only

MINIVLAR 30 
ethinyl estradiol, levonorgestrel tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72689-0011
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ETHINYL ESTRADIOL (ETHINYL ESTRADIOL) ETHINYL ESTRADIOL0.03 mg
LEVONORGESTREL (LEVONORGESTREL) LEVONORGESTREL0.15 mg
Inactive Ingredients
Ingredient NameStrength
STEARIC ACID 
STARCH, CORN 
POLYETHYLENE GLYCOL 6000 
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize5mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:72689-0011-121 TABLET in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/21/2018
Labeler - OASIS TRADING (689991468)
Registrant - OASIS TRADING (689991468)
Establishment
NameAddressID/FEIOperations
OASIS TRADING689991468manufacture(72689-0011), label(72689-0011)

 
OASIS TRADING

Further information

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