NDC 53002-1775
VelivetTriphasic Regimen 0.1 mg / 0.025 mg kit
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0555-9051.
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
- RPK Pharmaceuticals, Inc., Union City, California, United States · relabels it
Recalls
- Jun 17, 2014 · Class III · Teva Pharmaceuticals USA
Failed Impurities/Degradation Specifications: out of specification impurity test results.
Lots: Lot 33805449A, Exp. 12/14
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
- 0.1 mg / 0.025 mg
- Approval
- ANDA ANDA076455
- On the market since
- Mar 1, 2004
- Package NDCs
53002-1775-153002-1775-353002-1775-6- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2023
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