NDC 53002-1600
Azurette 0.02 mg / 0.15 mg kit
On the label: RPK Pharmaceuticals, Inc.. It's repackaged from NDC 51862-072, made by Mayne Pharma Inc. (Azurette). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it and relabels it). 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 RPK Pharmaceuticals, Inc. names for other drugs.
Product details
- Generic drug
- Desogestrel and Ethinyl Estradiol: every company that makes it
- Form
- kit
- Strength
- 0.02 mg / 0.15 mg
- Approval
- ANDA ANDA075863
- On the market since
- Nov 14, 2016
- Package NDCs
53002-1600-153002-1600-353002-1600-6- Official label
- DailyMed (National Library of Medicine), updated Dec 15, 2020
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