Drugplain

Aurovela Fe 1/20

Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate · KIT · Aurobindo Pharma Limited

No Recall History
Plain English

Aurovela Fe 1/20 is a kit containing norethindrone acetate and ethinyl estradiol and ferrous fumarate. Manufactured by Aurobindo Pharma Limited.

Key Facts

Brand Name
Aurovela Fe 1/20
Generic Name
Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate
NDC Code (Product)
65862-940
Manufacturer
Aurobindo Pharma Limited
Dosage Form
KIT
Marketing Status
Application #
ANDA207505
Marketing Start
06/16/2017

Recall History

No Recall History

Side Effects Reported to FDA

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

product dose omission issue15 reports
headache9 reports
nausea8 reports
rash7 reports
dermatitis atopic6 reports
fatigue5 reports
pruritus5 reports
vomiting4 reports
abdominal discomfort3 reports
abdominal distension3 reports

Frequently Asked Questions

What is Aurovela Fe 1/20 used for?

Aurovela Fe 1/20 contains Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate. It is a kit taken as directed. Consult your doctor for specific uses.

Is Aurovela Fe 1/20 a controlled substance?

Aurovela Fe 1/20 is not classified as a controlled substance by the DEA.

What is the generic name for Aurovela Fe 1/20?

The generic name for Aurovela Fe 1/20 is Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate. There are 11 other brand versions of Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate.

What is the NDC code for Aurovela Fe 1/20 ?

The NDC (National Drug Code) for Aurovela Fe 1/20 is 65862-940, listed by Aurobindo Pharma Limited.

Product NDC

65862-940

Package NDC

65862-940-58

Other Norethindrone Brands

See all →

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

Data from openFDA · Public domain (CC0 1.0)