Junel Fe 1/20

Active Ingredient(s): Ethinyl Estradiol + Norethindrone Acetate
FDA Approved: * September 18, 2003
Pharm Company: * BARR
Category: Birth Control / Contraceptive

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Junel Fe 1/20 Overview

Ethinylestradiol/norethisterone acetate (brand names Estrostep, Gildess, Junel, Loestrin, Microgestin, Minastrin, many others) is a combination of the estrogen ethinylestradiol and the progestin norethisterone acetate (norethindrone acetate) which is marketed under a large number of brand names throughout the world for use as a combined oral contraceptive.[1][additional citation(s) needed] In addition, the combination is marketed in the United States under the brand name FemHRT for use in hor...

Read more Junel Fe 1/20 Details
Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Junel

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NDC Database Records for Junel Fe 1/20: (3 results)

Sorted by National Drug Code

• 0555-9026 Junel Fe 1/20 28 Day Pack by Barr Laboratories Inc.
• 54868-5326 Junel Fe 1/20 28 Day Pack by Physicians Total Care, Inc.
• 68788-6832 Junel Fe 1/20 Kit by Preferred Pharmaceuticals Inc.

Drugs with one or more similar ingredients: (194 results)

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