NDC 50090-1395
Viorele 0.02 mg / 0.15 mg kit
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-318.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Recalls
- Sep 3, 2025 · Class II · Glenmark Pharmaceuticals Inc., USA
Failed Impurities/Degradation Specifications
Lots: Batch number 20230733, Exp Date: October 2025
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
- 0.02 mg / 0.15 mg
- Approval
- ANDA ANDA091346
- On the market since
- Apr 4, 2012
- Package NDCs
50090-1395-0- Official label
- DailyMed (National Library of Medicine), updated Jun 23, 2026
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