NDC 72189-215
Junel FE 1 mg / 20 ug tablet
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0555-9025.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- Direct Rx, Dawsonville, GA, United States · relabels it
Recalls
- Mar 15, 2013 · Class III · Teva Pharmaceuticals USA, Inc.
Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Benzene Sulfonamide (NBBS) was detected during impurity testing
Lots: NDC 0555-9028-58, Lot numbers 33802123A, exp 4/2013; 33802202A, exp 5/2013; 33802203A, exp 5/2013; and 33802204A, exp 5/2013.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ethinyl Estradiol and Norethindrone: every company that makes it
- Form
- tablet, oral
- Strength
- 1 mg / 20 ug
- Approval
- ANDA ANDA076380
- On the market since
- Oct 6, 2021
- Package NDCs
72189-215-28- Official label
- DailyMed (National Library of Medicine), updated Mar 17, 2026
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