NDC 42254-242
Junel Fe 1.5/30 30 ug / 1.5 mg kit
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0555-9028.
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
- Dispensing Solutions Inc., Santa Ana, California, United States · repackages it and relabels it
- Keltman Pharmaceuticals Inc., Location not on file · repackages it
- PSS World Medical, Inc., Olathe, Kansas, United States · repackages it
- Rebel Distributors Corp., Location not on file · repackages it and relabels it
- Script Pak, Location not on file · repackages it and relabels it
- Stat Rx USA, Location not on file · repackages 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
- kit
- Strength
- 30 ug / 1.5 mg
- Approval
- ANDA ANDA076064
- On the market since
- Jan 21, 2011
- Package NDCs
42254-242-28- Official label
- DailyMed (National Library of Medicine), updated Jun 13, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?