Drugplain

Junel Fe 1/20

norethindrone acetate and ethinyl estradiol, and ferrous fumarate · KIT · Preferred Pharmaceuticals Inc.

No Recall History
Plain English

Junel Fe 1/20 is a kit containing norethindrone acetate and ethinyl estradiol, and ferrous fumarate. Manufactured by Preferred Pharmaceuticals Inc..

Key Facts

Brand Name
Junel Fe 1/20
Generic Name
norethindrone acetate and ethinyl estradiol, and ferrous fumarate
NDC Code (Product)
68788-6832
Manufacturer
Preferred Pharmaceuticals Inc.
Dosage Form
KIT
Marketing Status
Application #
ANDA076081
Marketing Start
11/21/2016

Recall History

No Recall History

Frequently Asked Questions

What is Junel Fe 1/20 used for?

Junel 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 Junel Fe 1/20 a controlled substance?

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

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

The generic name for Junel Fe 1/20 is norethindrone acetate and ethinyl estradiol, and ferrous fumarate. There are 5 other brand versions of norethindrone acetate and ethinyl estradiol, and ferrous fumarate.

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

The NDC (National Drug Code) for Junel Fe 1/20 is 68788-6832, listed by Preferred Pharmaceuticals Inc..

Product NDC

68788-6832

Package NDC

68788-6832-2

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

Data from openFDA · Public domain (CC0 1.0)