Drugplain

ZAFEMY 35 ug/d

Norelgestromin and Ethinyl Estradiol · PATCH · Bryant Ranch Prepack

No Recall History
Plain English

Zafemy is a birth control patch that releases hormones through your skin to prevent pregnancy. It contains norelgestromin and ethinyl estradiol and is worn on the body as a transdermal patch.

Key Facts

Brand Name
ZAFEMY
Generic Name
Norelgestromin and Ethinyl Estradiol
NDC Code (Product)
72162-2220
Manufacturer
Bryant Ranch Prepack
Strength
35 ug/d
Dosage Form
PATCH
Route
TRANSDERMAL
Marketing Status
Application #
ANDA213950
Drug Class
Estrogen [EPC]; Progestin [EPC]
Marketing Start
06/28/2020

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

product adhesion issue19 reports
product substitution issue13 reports
intermenstrual bleeding8 reports
nausea6 reports
device adhesion issue4 reports
drug ineffective4 reports
dysmenorrhoea4 reports
headache4 reports
incorrect dose administered4 reports
injection site pain4 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

1 INDICATIONS AND USAGE ZAFEMY is indicated for the prevention of pregnancy in women with a body mass index (BMI) < 30 kg/m 2 for whom a combined hormonal contraceptive is appropriate. Limitations of Use: ZAFEMY may be less effective in preventing pregnancy in women who weigh 198 lbs (90 kg) or more. ZAFEMY is contraindicated for use in women with BMI ≥ 30 kg/m 2 [see Contraindications (4) , Warnings and Precautions (5.1) and Clinical Studies (14) ]. ZAFEMY ® is an estrogen/progestin combination hormonal contraceptive (CHC), indicated for the prevention of pregnancy in women with a BMI < 30 kg/m 2 for whom a combined hormonal contraceptive is appropriate. (1) Limitations of Use : ZAFEMY may be less effective in preventing pregnancy in women at or above 198 lbs (90 kg). ( 1 , 4 , 14 )

Dosage & Administration

2 DOSAGE AND ADMINISTRATION To achieve maximum contraceptive effectiveness, ZAFEMY must be used exactly as directed. Complete instructions to facilitate patient counseling on proper system usage may be found in the FDA-Approved Patient Labeling. ZAFEMY uses a 28-day (four-week) cycle. Apply a new patch to the upper outer arm, abdomen, buttock or back each week for three weeks (21 total days). Week Four is patch-free. (2.1, 2.3) Apply each new patch on the same day of the week. Wear only one patch at a time. (2.1) Do not cut or alter the patch in any way. (2.1) 2.1 How to Use ZAFEMY The ZAFEMY transdermal system uses a 28-day (four-week) cycle. A new patch is applied each week for three weeks (21 total days). Week Four is patch-free. Withdrawal bleeding is expected during this time. Every new patch should be applied on the same day of the week. This day is known as the “Patch Change Day.” For example, if the first patch is applied on a Monday, all subsequent patches should be applied on a Monday. Only one patch should be worn at a time. Do not cut, damage or alter the ZAFEMY patch in any way. If the ZAFEMY patch is cut, damaged or altered in size, contraceptive efficacy may be impai

Contraindications

4 CONTRAINDICATIONS ZAFEMY is contraindicated in females who are known to have or develop the following conditions: At high risk of arterial or venous thromboembolic events. Examples include women who: Smoke, if over age 35 [see Boxed Warning , and Warnings and Precautions (5.1) ] Have deep vein thrombosis or pulmonary embolism, now or in the past [see Warnings and Precautions (5.1) ] Have inherited or acquired hypercoagulopathies [see Warnings and Precautions (5.1) ] Have cerebrovascular disease [see Warnings and Precautions (5.1) ] Have coronary artery disease [see Warnings and Precautions (5.1) ] Have thrombogenic valvular or thrombogenic rhythm diseases of the heart (for example, subacute bacterial endocarditis with valvular disease, or atrial fibrillation) [see Warnings and Precautions (5.1) ] Have uncontrolled hypertension [see Warnings and Precautions (5.5) ] Have diabetes mellitus with vascular disease [see Warnings and Precautions (5.7) ] Have headaches with focal neurological symptoms or have migraine headaches with aura Women over age 35 with any migraine headaches [see Warnings and Precautions (5.8) ] Body Mass Index ≥ 30 kg/m 2 [see Warnings and Precautions (5.1) ] Liv

Drug Interactions

7 DRUG INTERACTIONS Consult the labeling of concurrently-used drugs to obtain further information about interactions with hormonal contraceptives or the potential for enzyme alterations. Drugs or herbal products that induce certain enzymes (for example CYP3A4) may decrease the effectiveness of CHCs or increase breakthrough bleeding. Counsel patients to use a back-up or alternative method of contraception when enzyme inducers are used with CHCs. (7.1) 7.1 Effects of Other Drugs on Combined Hormonal Contraceptives Substances Decreasing the Plasma Concentrations of CHCs and Potentially Diminishing the Efficacy of CHCs: Drugs or herbal products that induce certain enzymes, including cytochrome P450 3A4 (CYP3A4), may decrease the plasma concentrations of CHCs and potentially diminish the effectiveness of CHCs or increase breakthrough bleeding. Some drugs or herbal products that may decrease the effectiveness of hormonal contraceptives include phenytoin, barbiturates, carbamazepine, bosentan, felbamate, griseofulvin, oxcarbazepine, rifampicin, topiramate, rifabutin, rufinamide, aprepitant, and products containing St. John’s wort. Interactions between hormonal contraceptives and other dru

Adverse Reactions

6 ADVERSE REACTIONS The following serious adverse reactions with the use of combination hormonal contraceptives, including ZAFEMY, are discussed elsewhere in the labeling: Serious cardiovascular events and stroke [see Boxed Warning and Warnings and Precautions (5.1) ] Vascular events, including venous and arterial thromboembolic events [see Warnings and Precautions (5.1) ] Liver disease [see Warnings and Precautions (5.3) ] Adverse reactions commonly reported by users of combination hormonal contraceptives are: Irregular uterine bleeding Nausea Breast tenderness Headache The most frequent adverse reactions reported during clinical trials (≥ 5%) were breast symptoms, nausea/vomiting, headache, application site disorder, abdominal pain, dysmenorrhea, vaginal bleeding and menstrual disorders, and mood, affect and anxiety disorders. (6.1) To report SUSPECTED ADVERSE REACTIONS, contact Amneal Pharmaceuticals at 1-877-835-5472 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the cli

Frequently Asked Questions

What is ZAFEMY used for?

Zafemy is a birth control patch that releases hormones through your skin to prevent pregnancy. It contains norelgestromin and ethinyl estradiol and is worn on the body as a transdermal patch.

Is ZAFEMY a controlled substance?

ZAFEMY is not classified as a controlled substance by the DEA.

What is the generic name for ZAFEMY?

The generic name for ZAFEMY is Norelgestromin and Ethinyl Estradiol. There are 4 other brand versions of Norelgestromin and Ethinyl Estradiol.

What is the NDC code for ZAFEMY 35 ug/d?

The NDC (National Drug Code) for ZAFEMY 35 ug/d is 72162-2220, listed by Bryant Ranch Prepack.

Product NDC

72162-2220

Package NDC

72162-2220-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)