NDC 50090-2481
Apri28 Day 0.03 mg / 0.15 mg kit
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0555-9043.
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
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Recalls
- Jun 17, 2014 · Class III · Teva Pharmaceuticals USA
Failed Impurities/Degradation Specifications: out of specification impurity test results.
Lots: Lot 3805324A Exp. 11/14
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Desogestrel and Ethinyl Estradiol: every company that makes it
- Form
- kit
- Strength
- 0.03 mg / 0.15 mg
- Approval
- ANDA ANDA075256
- On the market since
- Oct 22, 1999
- Package NDCs
50090-2481-0- Official label
- DailyMed (National Library of Medicine), updated Jun 12, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?