NDC 53002-1735
drospirenone and ethinyl estradiol 3 mg / 0.02 mg kit
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-720.
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
- RPK Pharmaceuticals, Inc., Union City, California, United States · relabels it
Product details
- Generic drug
- Drospirenone and Ethinyl Estradiol: every company that makes it
- Form
- kit
- Strength
- 3 mg / 0.02 mg
- Approval
- ANDA ANDA204296
- On the market since
- Aug 17, 2015
- Package NDCs
53002-1735-153002-1735-353002-1735-6- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2023
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